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rs587777001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777001(G;G)
Make rs587777001(G;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position26501138
GeneKCTD1
is asnp
is mentioned by
dbSNPrs587777001
ebirs587777001
HLIrs587777001
Exacrs587777001
Varsomers587777001
Maprs587777001
PheGenIrs587777001
hapmaprs587777001
1000 genomesrs587777001
hgdprs587777001
ensemblrs587777001
gopubmedrs587777001
geneviewrs587777001
scholarrs587777001
googlers587777001
pharmgkbrs587777001
gwascentralrs587777001
openSNPrs587777001
23andMers587777001
23andMe allrs587777001
SNP Nexus

SNPshotrs587777001
SNPdbers587777001
MSV3drs587777001
GWAS Ctlgrs587777001
Max Magnitude0
ClinVar
Risk rs587777001(G;G)
Alt rs587777001(G;G)
Reference rs587777001(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.24081102T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000049297.3,