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rs1805031

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1805031(G;T)
Make rs1805031(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position151880879
GeneCACNB4
is asnp
is mentioned by
dbSNPrs1805031
ebirs1805031
HLIrs1805031
Exacrs1805031
Varsomers1805031
Maprs1805031
PheGenIrs1805031
hapmaprs1805031
1000 genomesrs1805031
hgdprs1805031
ensemblrs1805031
gopubmedrs1805031
geneviewrs1805031
scholarrs1805031
googlers1805031
pharmgkbrs1805031
gwascentralrs1805031
openSNPrs1805031
23andMers1805031
23andMe allrs1805031
SNP Nexus

SNPshotrs1805031
SNPdbers1805031
MSV3drs1805031
GWAS Ctlgrs1805031
GMAF0.0004591
Max Magnitude0
OMIM601949
Desc
Variant0002
Relatedalso
ClinVar
Risk rs1805031(T;T)
Alt rs1805031(T;T)
Reference rs1805031(G;G)
Significance Other
Disease Epilepsy Episodic ataxia not specified
Variation info
Gene CACNB4
CLNDBN Epilepsy, idiopathic generalized 9 Episodic ataxia, type 5 not specified
Reversed 1
HGVS NC_000002.11:g.152737393C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008046.3, RCV000008047.3, RCV000186828.2,