{{Rsnum
|rsid=34396614
|Gene=MYLK2
|Chromosome=20
|position=31820503
|Orientation=plus
|GMAF=0.01377
|Gene_s=MYLK2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=34396614
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=30408306
|CHROM=20
|GMAF=0.0137
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050068000000140516100100
|GENEINFO=MYLK2:85366
|GENE_NAME=MYLK2
|GENE_ID=85366
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.30408306C>G
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Cardiomyopathy; AllHighlyPenetrant
|Disease=Cardiomyopathy; AllHighlyPenetrant
|Tags=PM;PMC;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9862; 0.01377
|CLNACC=RCV000030331.1; RCV000039788.1
|CLNDSDB=MedGen:SNOMED_CT; MedGen
|CLNDSDBID=C0878544:85898001; CN169374
|COMMON=1
}}{{PMID Auto
|PMID=17344846
|Title=Patterns of somatic mutation in human cancer genomes.
|OA=1
}}{{GET Evidence
|gene=MYLK2
|aa_change=Pro144Ala
|aa_change_short=P144A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs34396614
|overall_frequency_n=165
|overall_frequency_d=10756
|overall_frequency=0.0153403
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=1
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.998
|nblosum100=2
|autoscore=2
|webscore=N
}}