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rs121964942

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964942(A;A)
Make rs121964942(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113149014
GeneF10
is asnp
is mentioned by
dbSNPrs121964942
ebirs121964942
HLIrs121964942
Exacrs121964942
Varsomers121964942
Maprs121964942
PheGenIrs121964942
hapmaprs121964942
1000 genomesrs121964942
hgdprs121964942
ensemblrs121964942
gopubmedrs121964942
geneviewrs121964942
scholarrs121964942
googlers121964942
pharmgkbrs121964942
gwascentralrs121964942
openSNPrs121964942
23andMers121964942
23andMe allrs121964942
SNP Nexus

SNPshotrs121964942
SNPdbers121964942
MSV3drs121964942
GWAS Ctlgrs121964942
Max Magnitude0
OMIM227600
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121964942(A;A)
Alt rs121964942(A;A)
Reference rs121964942(G;G)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113803328G>A
CLNSRC
CLNACC