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rs121964939

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964939(A;A)
Make rs121964939(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113129541
GeneF10
is asnp
is mentioned by
dbSNPrs121964939
ebirs121964939
HLIrs121964939
Exacrs121964939
Varsomers121964939
Maprs121964939
PheGenIrs121964939
hapmaprs121964939
1000 genomesrs121964939
hgdprs121964939
ensemblrs121964939
gopubmedrs121964939
geneviewrs121964939
scholarrs121964939
googlers121964939
pharmgkbrs121964939
gwascentralrs121964939
openSNPrs121964939
23andMers121964939
23andMe allrs121964939
SNP Nexus

SNPshotrs121964939
SNPdbers121964939
MSV3drs121964939
GWAS Ctlgrs121964939
Max Magnitude0
OMIM227600
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121964939(A;A)
Alt rs121964939(A;A)
Reference rs121964939(G;G)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113783855G>A
CLNSRC
CLNACC