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rs121909761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909761(A;A)
Make rs121909761(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position90705508
GeneGPR98
is asnp
is mentioned by
dbSNPrs121909761
ebirs121909761
HLIrs121909761
Exacrs121909761
Varsomers121909761
Maprs121909761
PheGenIrs121909761
hapmaprs121909761
1000 genomesrs121909761
hgdprs121909761
ensemblrs121909761
gopubmedrs121909761
geneviewrs121909761
scholarrs121909761
googlers121909761
pharmgkbrs121909761
gwascentralrs121909761
openSNPrs121909761
23andMers121909761
23andMe allrs121909761
SNP Nexus

SNPshotrs121909761
SNPdbers121909761
MSV3drs121909761
GWAS Ctlgrs121909761
Max Magnitude0
OMIM602851
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909761(A;A)
Alt rs121909761(A;A)
Reference rs121909761(C;C)
Significance Pathogenic
Disease Febrile seizures
Variation info
Gene GPR98 ADGRV1
CLNDBN Febrile seizures, familial, 4
Reversed 0
HGVS NC_000005.9:g.90001325C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007199.3,