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rs587777003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777003(C;T)
Make rs587777003(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position26476639
GeneKCTD1
is asnp
is mentioned by
dbSNPrs587777003
ebirs587777003
HLIrs587777003
Exacrs587777003
Varsomers587777003
Maprs587777003
PheGenIrs587777003
hapmaprs587777003
1000 genomesrs587777003
hgdprs587777003
ensemblrs587777003
gopubmedrs587777003
geneviewrs587777003
scholarrs587777003
googlers587777003
pharmgkbrs587777003
gwascentralrs587777003
openSNPrs587777003
23andMers587777003
23andMe allrs587777003
SNP Nexus

SNPshotrs587777003
SNPdbers587777003
MSV3drs587777003
GWAS Ctlgrs587777003
Max Magnitude0
ClinVar
Risk rs587777003(T;T)
Alt rs587777003(T;T)
Reference rs587777003(C;C)
Significance Pathogenic
Disease Scalp ear nipple syndrome
Variation info
Gene KCTD1
CLNDBN Scalp ear nipple syndrome
Reversed 0
HGVS NC_000018.9:g.24056603C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049299.3,