Have questions? Visit https://www.reddit.com/r/SNPedia

rs121907960

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
(TCT;TCT) 0 common in clinvar
(TTC;TTC) 0 common in complete genomics
Make rs121907960(-;-)
Make rs121907960(-;TTC)
ReferenceGRCh38 38.1/141
Chromosome15
Position72349153
GeneHEXA
is asnp
is mentioned by
dbSNPrs121907960
ebirs121907960
HLIrs121907960
Exacrs121907960
Varsomers121907960
Maprs121907960
PheGenIrs121907960
hapmaprs121907960
1000 genomesrs121907960
hgdprs121907960
ensemblrs121907960
gopubmedrs121907960
geneviewrs121907960
scholarrs121907960
googlers121907960
pharmgkbrs121907960
gwascentralrs121907960
openSNPrs121907960
23andMers121907960
23andMe allrs121907960
SNP Nexus

SNPshotrs121907960
SNPdbers121907960
MSV3drs121907960
GWAS Ctlgrs121907960
Max Magnitude0
OMIM606869
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121907960(;)
Alt rs121907960(;)
Reference rs121907960(CTT;CTT)
Significance Other
Disease Tay-Sachs disease
Variation info
Gene HEXA
CLNDBN Tay-Sachs disease
Reversed 1
HGVS NC_000015.9:g.72641489_72641491delAAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000169148.2,