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rs587777000

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777000(G;T)
Make rs587777000(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position26501137
GeneKCTD1
is asnp
is mentioned by
dbSNPrs587777000
ebirs587777000
HLIrs587777000
Exacrs587777000
Varsomers587777000
Maprs587777000
PheGenIrs587777000
hapmaprs587777000
1000 genomesrs587777000
hgdprs587777000
ensemblrs587777000
gopubmedrs587777000
geneviewrs587777000
scholarrs587777000
googlers587777000
pharmgkbrs587777000
gwascentralrs587777000
openSNPrs587777000
23andMers587777000
23andMe allrs587777000
SNP Nexus

SNPshotrs587777000
SNPdbers587777000
MSV3drs587777000
GWAS Ctlgrs587777000
Max Magnitude0
ClinVar
Risk rs587777000(A,T;A,T)
Alt rs587777000(A,T;A,T)
Reference rs587777000(G;G)
Significance Pathogenic
Disease Scalp ear nipple syndrome
Variation info
Gene KCTD1
CLNDBN Scalp ear nipple syndrome
Reversed 0
HGVS NC_000018.9:g.24081101G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049296.3,