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rs756953958

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756953958(A;A)
Make rs756953958(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position10544100
GeneMYHAS, MYH2
is asnp
is mentioned by
dbSNPrs756953958
ebirs756953958
HLIrs756953958
Exacrs756953958
Varsomers756953958
Maprs756953958
PheGenIrs756953958
hapmaprs756953958
1000 genomesrs756953958
hgdprs756953958
ensemblrs756953958
gopubmedrs756953958
geneviewrs756953958
scholarrs756953958
googlers756953958
pharmgkbrs756953958
gwascentralrs756953958
openSNPrs756953958
23andMers756953958
23andMe allrs756953958
SNP Nexus

SNPshotrs756953958
SNPdbers756953958
MSV3drs756953958
GWAS Ctlgrs756953958
Max Magnitude0
ClinVar
Risk rs756953958(A;A)
Alt rs756953958(A;A)
Reference rs756953958(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.10447417G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000162324.2,