Have questions? Visit https://www.reddit.com/r/SNPedia

rs542835031

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs542835031(A;A)
Make rs542835031(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome21
Position34370683
GeneKCNE2, LOC105372791
is asnp
is mentioned by
dbSNPrs542835031
ebirs542835031
HLIrs542835031
Exacrs542835031
Varsomers542835031
Maprs542835031
PheGenIrs542835031
hapmaprs542835031
1000 genomesrs542835031
hgdprs542835031
ensemblrs542835031
gopubmedrs542835031
geneviewrs542835031
scholarrs542835031
googlers542835031
pharmgkbrs542835031
gwascentralrs542835031
openSNPrs542835031
23andMers542835031
23andMe allrs542835031
SNP Nexus

SNPshotrs542835031
SNPdbers542835031
MSV3drs542835031
GWAS Ctlgrs542835031
Max Magnitude0
ClinVar
Risk rs542835031(A;A)
Alt rs542835031(A;A)
Reference rs542835031(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNE2
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.35742982G>A
CLNSRC
CLNACC RCV000170961.2,