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rs10030601

From SNPedia

Orientationplus
Stabilizedplus
Make rs10030601(C;C)
Make rs10030601(C;T)
Make rs10030601(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position149804060
GeneIGHVII-53-1
is asnp
is mentioned by
dbSNPrs10030601
ebirs10030601
HLIrs10030601
Exacrs10030601
Varsomers10030601
Maprs10030601
PheGenIrs10030601
hapmaprs10030601
1000 genomesrs10030601
hgdprs10030601
ensemblrs10030601
gopubmedrs10030601
geneviewrs10030601
scholarrs10030601
googlers10030601
pharmgkbrs10030601
gwascentralrs10030601
openSNPrs10030601
23andMers10030601
23andMe allrs10030601
SNP Nexus

SNPshotrs10030601
SNPdbers10030601
MSV3drs10030601
GWAS Ctlgrs10030601
GMAF0.2815
Max Magnitude
GWAS snp
PMID [PMID 22949513]
Trait Epilepsy (generalized)
Title Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
Risk Allele C
P-val 1E-6
Odds Ratio 1.58 [1.29-1.93]