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rs121964943

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121964943(A;G)
Make rs121964943(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113129521
GeneF10
is asnp
is mentioned by
dbSNPrs121964943
ebirs121964943
HLIrs121964943
Exacrs121964943
Varsomers121964943
Maprs121964943
PheGenIrs121964943
hapmaprs121964943
1000 genomesrs121964943
hgdprs121964943
ensemblrs121964943
gopubmedrs121964943
geneviewrs121964943
scholarrs121964943
googlers121964943
pharmgkbrs121964943
gwascentralrs121964943
openSNPrs121964943
23andMers121964943
23andMe allrs121964943
SNP Nexus

SNPshotrs121964943
SNPdbers121964943
MSV3drs121964943
GWAS Ctlgrs121964943
Max Magnitude0
OMIM227600
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121964943(G;G)
Alt rs121964943(G;G)
Reference rs121964943(A;A)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113783835A>G
CLNSRC
CLNACC