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rs878853125

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853125(C;T)
Make rs878853125(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome18
Position26501178
GeneKCTD1
is asnp
is mentioned by
dbSNPrs878853125
ebirs878853125
HLIrs878853125
Exacrs878853125
Varsomers878853125
Maprs878853125
PheGenIrs878853125
hapmaprs878853125
1000 genomesrs878853125
hgdprs878853125
ensemblrs878853125
gopubmedrs878853125
geneviewrs878853125
scholarrs878853125
googlers878853125
pharmgkbrs878853125
gwascentralrs878853125
openSNPrs878853125
23andMers878853125
23andMe allrs878853125
SNP Nexus

SNPshotrs878853125
SNPdbers878853125
MSV3drs878853125
GWAS Ctlgrs878853125
Max Magnitude0
ClinVar
Risk rs878853125(T;T)
Alt rs878853125(T;T)
Reference rs878853125(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.24081142G>A
CLNSRC
CLNACC RCV000224008.1,