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rs797044880

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044880(G;T)
Make rs797044880(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position8512588
GeneLOC102724262, MYH10
is asnp
is mentioned by
dbSNPrs797044880
ebirs797044880
HLIrs797044880
Exacrs797044880
Varsomers797044880
Maprs797044880
PheGenIrs797044880
hapmaprs797044880
1000 genomesrs797044880
hgdprs797044880
ensemblrs797044880
gopubmedrs797044880
geneviewrs797044880
scholarrs797044880
googlers797044880
pharmgkbrs797044880
gwascentralrs797044880
openSNPrs797044880
23andMers797044880
23andMe allrs797044880
SNP Nexus

SNPshotrs797044880
SNPdbers797044880
MSV3drs797044880
GWAS Ctlgrs797044880
Max Magnitude0
ClinVar
Risk rs797044880(T;T)
Alt rs797044880(T;T)
Reference rs797044880(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene MYH10
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000017.10:g.8415906C>A
CLNSRC
CLNACC RCV000190694.1,