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rs762121316

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762121316(A;A)
Make rs762121316(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position10533379
GeneMYHAS, MYH2
is asnp
is mentioned by
dbSNPrs762121316
ebirs762121316
HLIrs762121316
Exacrs762121316
Varsomers762121316
Maprs762121316
PheGenIrs762121316
hapmaprs762121316
1000 genomesrs762121316
hgdprs762121316
ensemblrs762121316
gopubmedrs762121316
geneviewrs762121316
scholarrs762121316
googlers762121316
pharmgkbrs762121316
gwascentralrs762121316
openSNPrs762121316
23andMers762121316
23andMe allrs762121316
SNP Nexus

SNPshotrs762121316
SNPdbers762121316
MSV3drs762121316
GWAS Ctlgrs762121316
Max Magnitude0
ClinVar
Risk rs762121316(A;A)
Alt rs762121316(A;A)
Reference rs762121316(G;G)
Significance Pathogenic
Disease Inclusion body myopathy 3
Variation info
Gene MYH2 MYHAS
CLNDBN Inclusion body myopathy 3
Reversed 0
HGVS NC_000017.10:g.10436696G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162319.3,