{{Rsnum
|rsid=3848519
|Gene=FECH
|Chromosome=18
|position=57580104
|Orientation=plus
|GMAF=0.01607
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=FECH
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 1.8 | 98.2
| HCB | 0.0 | 3.7 | 96.3
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 3.4 | 96.6
| ASW | 0.0 | 1.8 | 98.2
| CHB | 0.0 | 3.7 | 96.3
| CHD | 0.0 | 3.7 | 96.3
| GIH | 0.0 | 9.9 | 90.1
| LWK | 0.0 | 4.6 | 95.4
| MEX | 0.0 | 7.1 | 92.9
| MKK | 0.0 | 1.3 | 98.7
| TSI | 0.0 | 3.0 | 97.0
| HapMapRevision=28
}}{{omim
|id=612386
|rsnum=3848519
|variant=0001
}}

{{ClinVar
|rsid=3848519
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=55247336
|CHROM=18
|GMAF=0.016
|dbSNPBuildID=108
|SSR=0
|SAO=0
|VP=0x050160000000150517110100
|GENEINFO=FECH:2235
|GENE_NAME=FECH
|GENE_ID=2235
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000018.9:g.55247336C>A
|CLNSIG=5
|Tags=PM;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;OM
|CAF=0.9839; 0.01607; .
|CLNACC=RCV000000578.1
|CLNDBN=Erythropoietic protoporphyria
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK100826:C0162568:177000:79278:51022005
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=612386.0001
|COMMON=1
|Disease=Erythropoietic protoporphyria
}}

{{GET Evidence
|gene=FECH
|aa_change=Gly55Cys
|aa_change_short=G55C
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3848519
|overall_frequency_n=191
|overall_frequency_d=10758
|overall_frequency=0.0177542
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|in_omim=Y
|genetests_testable=Y
|nblosum100=7
|autoscore=4
|webscore=N
|n_web_uneval=4
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}