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rs1064794856

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Carrier of a Tay-Sachs mutation
(G;G) 8.8 Tay-Sachs disease (predicted)
Chromosome15
Position72353108
GeneHEXA
is asnp
is mentioned by
dbSNPrs1064794856
dbSNP (old)rs1064794856
ClinGenrs1064794856
ebirs1064794856
HLIrs1064794856
Exacrs1064794856
Gnomadrs1064794856
Varsomers1064794856
Maprs1064794856
PheGenIrs1064794856
Biobankrs1064794856
1000 genomesrs1064794856
hgdprs1064794856
ensemblrs1064794856
gopubmedrs1064794856
geneviewrs1064794856
scholarrs1064794856
googlers1064794856
pharmgkbrs1064794856
gwascentralrs1064794856
openSNPrs1064794856
23andMers1064794856
23andMe allrs1064794856
SNPshotrs1064794856
SNPdbers1064794856
MSV3drs1064794856
GWAS Ctlgrs1064794856
Max Magnitude8.8
ClinVar
Risk Rs1064794856(G;G)
Alt Rs1064794856(G;G)
Reference Rs1064794856(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HEXA
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.72645449G>C
CLNSRC
CLNACC RCV000485524.1,