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rs774455945

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774455945(C;T)
Make rs774455945(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position43769027
GeneKCNN4
is asnp
is mentioned by
dbSNPrs774455945
ebirs774455945
HLIrs774455945
Exacrs774455945
Varsomers774455945
Maprs774455945
PheGenIrs774455945
hapmaprs774455945
1000 genomesrs774455945
hgdprs774455945
ensemblrs774455945
gopubmedrs774455945
geneviewrs774455945
scholarrs774455945
googlers774455945
pharmgkbrs774455945
gwascentralrs774455945
openSNPrs774455945
23andMers774455945
23andMe allrs774455945
SNP Nexus

SNPshotrs774455945
SNPdbers774455945
MSV3drs774455945
GWAS Ctlgrs774455945
Max Magnitude0
ClinVar
Risk rs774455945(T;T)
Alt rs774455945(T;T)
Reference rs774455945(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNN4
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.44273179C>T
CLNSRC
CLNACC RCV000239166.1,