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rs786204515

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204515(-;-)
Make rs786204515(-;A)
Make rs786204515(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position72349117
GeneHEXA
is asnp
is mentioned by
dbSNPrs786204515
ebirs786204515
HLIrs786204515
Exacrs786204515
Varsomers786204515
Maprs786204515
PheGenIrs786204515
hapmaprs786204515
1000 genomesrs786204515
hgdprs786204515
ensemblrs786204515
gopubmedrs786204515
geneviewrs786204515
scholarrs786204515
googlers786204515
pharmgkbrs786204515
gwascentralrs786204515
openSNPrs786204515
23andMers786204515
23andMe allrs786204515
SNP Nexus

SNPshotrs786204515
SNPdbers786204515
MSV3drs786204515
GWAS Ctlgrs786204515
Max Magnitude0
ClinVar
Risk rs786204515(A;A)
Alt rs786204515(A;A)
Reference rs786204515(;)
Significance Probable-Pathogenic
Disease Tay-Sachs disease
Variation info
Gene HEXA
CLNDBN Tay-Sachs disease
Reversed 1
HGVS NC_000015.9:g.72641459dupT
CLNSRC
CLNACC RCV000169207.1,