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rs121964929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121964929(A;A)
Make rs121964929(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113118527
GeneF7
is asnp
is mentioned by
dbSNPrs121964929
ebirs121964929
HLIrs121964929
Exacrs121964929
Varsomers121964929
Maprs121964929
PheGenIrs121964929
hapmaprs121964929
1000 genomesrs121964929
hgdprs121964929
ensemblrs121964929
gopubmedrs121964929
geneviewrs121964929
scholarrs121964929
googlers121964929
pharmgkbrs121964929
gwascentralrs121964929
openSNPrs121964929
23andMers121964929
23andMe allrs121964929
SNP Nexus

SNPshotrs121964929
SNPdbers121964929
MSV3drs121964929
GWAS Ctlgrs121964929
Max Magnitude0
OMIM227500
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121964929(A;A)
Alt rs121964929(A;A)
Reference rs121964929(G;G)
Significance Untested
Disease
Variation info
Gene F7
CLNDBN
Reversed 0
HGVS NC_000013.10:g.113772841G>A
CLNSRC
CLNACC