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rs797045096

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045096(-;-)
Make rs797045096(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position10529679
GeneMYHAS, MYH2
is asnp
is mentioned by
dbSNPrs797045096
ebirs797045096
HLIrs797045096
Exacrs797045096
Varsomers797045096
Maprs797045096
PheGenIrs797045096
hapmaprs797045096
1000 genomesrs797045096
hgdprs797045096
ensemblrs797045096
gopubmedrs797045096
geneviewrs797045096
scholarrs797045096
googlers797045096
pharmgkbrs797045096
gwascentralrs797045096
openSNPrs797045096
23andMers797045096
23andMe allrs797045096
SNP Nexus

SNPshotrs797045096
SNPdbers797045096
MSV3drs797045096
GWAS Ctlgrs797045096
Max Magnitude0
ClinVar
Risk rs797045096(;)
Alt rs797045096(;)
Reference rs797045096(A;A)
Significance Probable-Pathogenic
Disease Inclusion body myopathy 3
Variation info
Gene MYH2 MYHAS
CLNDBN Inclusion body myopathy 3
Reversed 1
HGVS NC_000017.10:g.10432996delT
CLNSRC
CLNACC RCV000190605.1,