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rs797044872

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044872(A;A)
Make rs797044872(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position50323685
GeneKCNC3
is asnp
is mentioned by
dbSNPrs797044872
ebirs797044872
HLIrs797044872
Exacrs797044872
Varsomers797044872
Maprs797044872
PheGenIrs797044872
hapmaprs797044872
1000 genomesrs797044872
hgdprs797044872
ensemblrs797044872
gopubmedrs797044872
geneviewrs797044872
scholarrs797044872
googlers797044872
pharmgkbrs797044872
gwascentralrs797044872
openSNPrs797044872
23andMers797044872
23andMe allrs797044872
SNP Nexus

SNPshotrs797044872
SNPdbers797044872
MSV3drs797044872
GWAS Ctlgrs797044872
Max Magnitude0
ClinVar
Risk rs797044872(A;A)
Alt rs797044872(A;A)
Reference rs797044872(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene KCNC3
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000019.9:g.50826942C>T
CLNSRC
CLNACC RCV000190682.1,