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rs201627778

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201627778(A;A)
Make rs201627778(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150948462
GeneKCNH2
is asnp
is mentioned by
dbSNPrs201627778
ebirs201627778
HLIrs201627778
Exacrs201627778
Varsomers201627778
Maprs201627778
PheGenIrs201627778
hapmaprs201627778
1000 genomesrs201627778
hgdprs201627778
ensemblrs201627778
gopubmedrs201627778
geneviewrs201627778
scholarrs201627778
googlers201627778
pharmgkbrs201627778
gwascentralrs201627778
openSNPrs201627778
23andMers201627778
23andMe allrs201627778
SNP Nexus

SNPshotrs201627778
SNPdbers201627778
MSV3drs201627778
GWAS Ctlgrs201627778
Max Magnitude0
ClinVar
Risk rs201627778(A,C;A,C)
Alt rs201627778(A,C;A,C)
Reference rs201627778(G;G)
Significance Other
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150645550G>A
CLNSRC
CLNACC RCV000171663.2,