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rs121964945

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964945(C;C)
Make rs121964945(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113129595
GeneF10
is asnp
is mentioned by
dbSNPrs121964945
ebirs121964945
HLIrs121964945
Exacrs121964945
Varsomers121964945
Maprs121964945
PheGenIrs121964945
hapmaprs121964945
1000 genomesrs121964945
hgdprs121964945
ensemblrs121964945
gopubmedrs121964945
geneviewrs121964945
scholarrs121964945
googlers121964945
pharmgkbrs121964945
gwascentralrs121964945
openSNPrs121964945
23andMers121964945
23andMe allrs121964945
SNP Nexus

SNPshotrs121964945
SNPdbers121964945
MSV3drs121964945
GWAS Ctlgrs121964945
Max Magnitude0
OMIM227600
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121964945(C;C)
Alt rs121964945(C;C)
Reference rs121964945(G;G)
Significance Untested
Disease
Variation info
Gene F10
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113783909G>C
CLNSRC
CLNACC