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rs121909715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909715(A;A)
Make rs121909715(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position121310819
GeneGSN
is asnp
is mentioned by
dbSNPrs121909715
dbSNP (old)rs121909715
ClinGenrs121909715
ebirs121909715
HLIrs121909715
Exacrs121909715
Gnomadrs121909715
Varsomers121909715
Maprs121909715
PheGenIrs121909715
Biobankrs121909715
1000 genomesrs121909715
hgdprs121909715
ensemblrs121909715
gopubmedrs121909715
geneviewrs121909715
scholarrs121909715
googlers121909715
pharmgkbrs121909715
gwascentralrs121909715
openSNPrs121909715
23andMers121909715
23andMe allrs121909715
SNP Nexus

SNPshotrs121909715
SNPdbers121909715
MSV3drs121909715
GWAS Ctlgrs121909715
Merged fromRs121909716
Max Magnitude0
OMIM137350
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909715(A;A) rs121909715(T;T)
Alt rs121909715(A;A) rs121909715(T;T)
Reference Rs121909715(G;G)
Significance Pathogenic
Disease Meretoja syndrome not provided
Variation info
Gene GSN
CLNDBN Meretoja syndrome not provided
Reversed 0
HGVS NC_000009.11:g.124073097G>A; NC_000009.11:g.124073097G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017564.25, RCV000489240.1, RCV000017565.27,