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rs121907984

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121907984(A;A)
Make rs121907984(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position74721131
GeneGFM2, HEXB
is asnp
is mentioned by
dbSNPrs121907984
ebirs121907984
HLIrs121907984
Exacrs121907984
Varsomers121907984
Maprs121907984
PheGenIrs121907984
hapmaprs121907984
1000 genomesrs121907984
hgdprs121907984
ensemblrs121907984
gopubmedrs121907984
geneviewrs121907984
scholarrs121907984
googlers121907984
pharmgkbrs121907984
gwascentralrs121907984
openSNPrs121907984
23andMers121907984
23andMe allrs121907984
SNP Nexus

SNPshotrs121907984
SNPdbers121907984
MSV3drs121907984
GWAS Ctlgrs121907984
Max Magnitude0
OMIM606873
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121907984(A;A)
Alt rs121907984(A;A)
Reference rs121907984(G;G)
Significance Non-pathogenic
Disease HEXOSAMINIDASE B not provided
Variation info
Gene HEXB GFM2
CLNDBN HEXOSAMINIDASE B, HEAT-LABILE POLYMORPHISM not provided
Reversed 0
HGVS NC_000005.9:g.74016956G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000004085.2, RCV000079061.4,