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rs587777002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777002(G;G)
Make rs587777002(G;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position26476603
GeneKCTD1
is asnp
is mentioned by
dbSNPrs587777002
ebirs587777002
HLIrs587777002
Exacrs587777002
Varsomers587777002
Maprs587777002
PheGenIrs587777002
hapmaprs587777002
1000 genomesrs587777002
hgdprs587777002
ensemblrs587777002
gopubmedrs587777002
geneviewrs587777002
scholarrs587777002
googlers587777002
pharmgkbrs587777002
gwascentralrs587777002
openSNPrs587777002
23andMers587777002
23andMe allrs587777002
SNP Nexus

SNPshotrs587777002
SNPdbers587777002
MSV3drs587777002
GWAS Ctlgrs587777002
Max Magnitude0
ClinVar
Risk rs587777002(G;G)
Alt rs587777002(G;G)
Reference rs587777002(T;T)
Significance Pathogenic
Disease Scalp ear nipple syndrome
Variation info
Gene KCTD1
CLNDBN Scalp ear nipple syndrome
Reversed 0
HGVS NC_000018.9:g.24056567T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000049298.3,