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rs121964940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121964940(C;T)
Make rs121964940(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position113149197
GeneF10
is asnp
is mentioned by
dbSNPrs121964940
ebirs121964940
HLIrs121964940
Exacrs121964940
Varsomers121964940
Maprs121964940
PheGenIrs121964940
hapmaprs121964940
1000 genomesrs121964940
hgdprs121964940
ensemblrs121964940
gopubmedrs121964940
geneviewrs121964940
scholarrs121964940
googlers121964940
pharmgkbrs121964940
gwascentralrs121964940
openSNPrs121964940
23andMers121964940
23andMe allrs121964940
SNP Nexus

SNPshotrs121964940
SNPdbers121964940
MSV3drs121964940
GWAS Ctlgrs121964940
Max Magnitude0
OMIM227600
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121964940(T;T)
Alt rs121964940(T;T)
Reference rs121964940(C;C)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113803511C>T
CLNSRC
CLNACC