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rs121964938

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964938(C;C)
Make rs121964938(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118770
GeneF7
is asnp
is mentioned by
dbSNPrs121964938
ebirs121964938
HLIrs121964938
Exacrs121964938
Varsomers121964938
Maprs121964938
PheGenIrs121964938
hapmaprs121964938
1000 genomesrs121964938
hgdprs121964938
ensemblrs121964938
gopubmedrs121964938
geneviewrs121964938
scholarrs121964938
googlers121964938
pharmgkbrs121964938
gwascentralrs121964938
openSNPrs121964938
23andMers121964938
23andMe allrs121964938
SNP Nexus

SNPshotrs121964938
SNPdbers121964938
MSV3drs121964938
GWAS Ctlgrs121964938
Max Magnitude0
OMIM227500
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121964938(C,G;C,G)
Alt rs121964938(C,G;C,G)
Reference rs121964938(T;T)
Significance Untested
Disease
Variation info
Gene F7
CLNDBN OMIM
Reversed 0
HGVS NC_000013.10:g.113773084T>C; NC_000013.10:g.113773084T>G
CLNSRC
CLNACC