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rs121964944

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964944(A;G)
Make rs121964944(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113129542
GeneF10
is asnp
is mentioned by
dbSNPrs121964944
ebirs121964944
HLIrs121964944
Exacrs121964944
Varsomers121964944
Maprs121964944
PheGenIrs121964944
hapmaprs121964944
1000 genomesrs121964944
hgdprs121964944
ensemblrs121964944
gopubmedrs121964944
geneviewrs121964944
scholarrs121964944
googlers121964944
pharmgkbrs121964944
gwascentralrs121964944
openSNPrs121964944
23andMers121964944
23andMe allrs121964944
SNP Nexus

SNPshotrs121964944
SNPdbers121964944
MSV3drs121964944
GWAS Ctlgrs121964944
Max Magnitude0
OMIM227600
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121964944(G;G)
Alt rs121964944(G;G)
Reference rs121964944(A;A)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113783856A>G
CLNSRC
CLNACC