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rs121964946

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964946(C;C)
Make rs121964946(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113147496
GeneF10
is asnp
is mentioned by
dbSNPrs121964946
ebirs121964946
HLIrs121964946
Exacrs121964946
Varsomers121964946
Maprs121964946
PheGenIrs121964946
hapmaprs121964946
1000 genomesrs121964946
hgdprs121964946
ensemblrs121964946
gopubmedrs121964946
geneviewrs121964946
scholarrs121964946
googlers121964946
pharmgkbrs121964946
gwascentralrs121964946
openSNPrs121964946
23andMers121964946
23andMe allrs121964946
SNP Nexus

SNPshotrs121964946
SNPdbers121964946
MSV3drs121964946
GWAS Ctlgrs121964946
Max Magnitude0
OMIM227600
Desc
Variant0012
Relatedalso
ClinVar
Risk rs121964946(C;C)
Alt rs121964946(C;C)
Reference rs121964946(G;G)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113801810G>C
CLNSRC
CLNACC