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rs786201023

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201023(C;C)
Make rs786201023(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position10523154
GeneMYHAS, MYH2
is asnp
is mentioned by
dbSNPrs786201023
ebirs786201023
HLIrs786201023
Exacrs786201023
Varsomers786201023
Maprs786201023
PheGenIrs786201023
hapmaprs786201023
1000 genomesrs786201023
hgdprs786201023
ensemblrs786201023
gopubmedrs786201023
geneviewrs786201023
scholarrs786201023
googlers786201023
pharmgkbrs786201023
gwascentralrs786201023
openSNPrs786201023
23andMers786201023
23andMe allrs786201023
SNP Nexus

SNPshotrs786201023
SNPdbers786201023
MSV3drs786201023
GWAS Ctlgrs786201023
Max Magnitude0
ClinVar
Risk rs786201023(C;C)
Alt rs786201023(C;C)
Reference rs786201023(T;T)
Significance Pathogenic
Disease Inclusion body myopathy 3
Variation info
Gene MYH2 MYHAS
CLNDBN Inclusion body myopathy 3
Reversed 1
HGVS NC_000017.10:g.10426471A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000162317.2,