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rs878853124

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853124(A;A)
Make rs878853124(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position26476617
GeneKCTD1
is asnp
is mentioned by
dbSNPrs878853124
ebirs878853124
HLIrs878853124
Exacrs878853124
Varsomers878853124
Maprs878853124
PheGenIrs878853124
hapmaprs878853124
1000 genomesrs878853124
hgdprs878853124
ensemblrs878853124
gopubmedrs878853124
geneviewrs878853124
scholarrs878853124
googlers878853124
pharmgkbrs878853124
gwascentralrs878853124
openSNPrs878853124
23andMers878853124
23andMe allrs878853124
SNP Nexus

SNPshotrs878853124
SNPdbers878853124
MSV3drs878853124
GWAS Ctlgrs878853124
Max Magnitude0
ClinVar
Risk rs878853124(A;A)
Alt rs878853124(A;A)
Reference rs878853124(C;C)
Significance Pathogenic
Disease Scalp ear nipple syndrome
Variation info
Gene KCTD1
CLNDBN Scalp ear nipple syndrome
Reversed 1
HGVS NC_000018.9:g.24056581G>T
CLNSRC
CLNACC RCV000224280.1,