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rs1060501889

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501889(-;-)
Make rs1060501889(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position162149210
GeneGABRG2
is asnp
is mentioned by
dbSNPrs1060501889
dbSNP (old)rs1060501889
ClinGenrs1060501889
ebirs1060501889
HLIrs1060501889
Exacrs1060501889
Gnomadrs1060501889
Varsomers1060501889
Maprs1060501889
PheGenIrs1060501889
Biobankrs1060501889
1000 genomesrs1060501889
hgdprs1060501889
ensemblrs1060501889
gopubmedrs1060501889
geneviewrs1060501889
scholarrs1060501889
googlers1060501889
pharmgkbrs1060501889
gwascentralrs1060501889
openSNPrs1060501889
23andMers1060501889
23andMe allrs1060501889
SNPshotrs1060501889
SNPdbers1060501889
MSV3drs1060501889
GWAS Ctlgrs1060501889
Max Magnitude0
ClinVar
Risk rs1060501889(-;-)
Alt rs1060501889(-;-)
Reference Rs1060501889(G;G)
Significance Probable-Pathogenic
Disease Epilepsy Familial febrile seizures 8
Variation info
Gene GABRG2
CLNDBN Epilepsy, childhood absence 2 Familial febrile seizures 8
Reversed 0
HGVS NC_000005.9:g.161576216delG
CLNSRC
CLNACC RCV000462535.1,