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rs121909716

From SNPedia

Merged intors121909715
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909716(G;T)
Make rs121909716(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position121310819
GeneGSN
is asnp
is mentioned by
dbSNPrs121909716
ebirs121909716
HLIrs121909716
Exacrs121909716
Varsomers121909716
Maprs121909716
PheGenIrs121909716
hapmaprs121909716
1000 genomesrs121909716
hgdprs121909716
ensemblrs121909716
gopubmedrs121909716
geneviewrs121909716
scholarrs121909716
googlers121909716
pharmgkbrs121909716
gwascentralrs121909716
openSNPrs121909716
23andMers121909716
23andMe allrs121909716
SNP Nexus

SNPshotrs121909716
SNPdbers121909716
MSV3drs121909716
GWAS Ctlgrs121909716
StatusMerged into rs121909715
Max Magnitude0
OMIM137350
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909716(T;T)
Alt rs121909716(T;T)
Reference rs121909716(G;G)
Significance Pathogenic
Disease
Variation info
Gene GSN
CLNDBN
Reversed 0
HGVS NC_000009.11:g.124073097G>T
CLNSRC
CLNACC