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rs370266293

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370266293(C;T)
Make rs370266293(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position72346679
GeneHEXA
is asnp
is mentioned by
dbSNPrs370266293
ebirs370266293
HLIrs370266293
Exacrs370266293
Varsomers370266293
Maprs370266293
PheGenIrs370266293
hapmaprs370266293
1000 genomesrs370266293
hgdprs370266293
ensemblrs370266293
gopubmedrs370266293
geneviewrs370266293
scholarrs370266293
googlers370266293
pharmgkbrs370266293
gwascentralrs370266293
openSNPrs370266293
23andMers370266293
23andMe allrs370266293
SNP Nexus

SNPshotrs370266293
SNPdbers370266293
MSV3drs370266293
GWAS Ctlgrs370266293
Max Magnitude0
ClinVar
Risk rs370266293(T;T)
Alt rs370266293(T;T)
Reference rs370266293(C;C)
Significance Pathogenic
Disease Tay-Sachs disease
Variation info
Gene HEXA
CLNDBN Tay-Sachs disease
Reversed 0
HGVS NC_000015.9:g.72639020C>G
CLNSRC
CLNACC RCV000202576.1,