{{Rsnum
|rsid=34231037
|Gene=KDR
|Chromosome=4
|position=55106779
|Orientation=plus
|GMAF=0.01377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=KDR
}}{{omim
|id=191306
|rsnum=34231037
|variant=0002
}}

{{ClinVar
|rsid=34231037
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=55972946
|CHROM=4
|GMAF=0.0137
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050260000000140516110100
|GENEINFO=KDR:3791
|GENE_NAME=KDR
|GENE_ID=3791
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.55972946A>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9862; 0.01377
|CLNACC=RCV000013111.1
|CLNDBN=Hemangioma, capillary infantile, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=191306.0002
|COMMON=1
|Disease=Hemangioma
}}

{{GET Evidence
|gene=KDR
|aa_change=Cys482Arg
|aa_change_short=C482R
|impact=pathogenic
|qualified_impact=Low clinical importance, Uncertain pathogenic
|inheritance=other
|quality_scores=Array
|dbsnp_id=rs34231037
|overall_frequency_n=225
|overall_frequency_d=10758
|overall_frequency=0.0209147
|n_genomes=2
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=1
|n_articles_annotated=1
|qualityscore_in_silico=1
|qualitycomment_in_silico=Y
|qualityscore_case_control=0
|qualitycomment_case_control=Y
|qualityscore_severity=1
|qualityscore_treatability=4
|in_omim=Y
|pph2_score=0.999
|nblosum100=8
|autoscore=4
|webscore=N
|variant_evidence=0
|clinical_importance=0
|summary_short=Hypothesized to cause a higher risk of benign neonatal hemangiomas (which are seen in 10% of children). However, observations lacked statistical significance.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}