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rs141016843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141016843(C;T)
Make rs141016843(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position39310983
GeneKCNK17
is asnp
is mentioned by
dbSNPrs141016843
ebirs141016843
HLIrs141016843
Exacrs141016843
Varsomers141016843
Maprs141016843
PheGenIrs141016843
hapmaprs141016843
1000 genomesrs141016843
hgdprs141016843
ensemblrs141016843
gopubmedrs141016843
geneviewrs141016843
scholarrs141016843
googlers141016843
pharmgkbrs141016843
gwascentralrs141016843
openSNPrs141016843
23andMers141016843
23andMe allrs141016843
SNP Nexus

SNPshotrs141016843
SNPdbers141016843
MSV3drs141016843
GWAS Ctlgrs141016843
Max Magnitude0
ClinVar
Risk rs141016843(T;T)
Alt rs141016843(T;T)
Reference rs141016843(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNK17
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.39278759C>T
CLNSRC ClinVar
CLNACC RCV000149444.1,