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rs1006615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1006615(C;T)
Make rs1006615(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130433393
GeneHMCN2
is asnp
is mentioned by
dbSNPrs1006615
ebirs1006615
HLIrs1006615
Exacrs1006615
Varsomers1006615
Maprs1006615
PheGenIrs1006615
hapmaprs1006615
1000 genomesrs1006615
hgdprs1006615
ensemblrs1006615
gopubmedrs1006615
geneviewrs1006615
scholarrs1006615
googlers1006615
pharmgkbrs1006615
gwascentralrs1006615
openSNPrs1006615
23andMers1006615
23andMe allrs1006615
SNP Nexus

SNPshotrs1006615
SNPdbers1006615
MSV3drs1006615
GWAS Ctlgrs1006615
GMAF0.3517
Max Magnitude0
[PMID 18936756] rs1006615 is associated with increased risk for schizophrenia in German and Scandinavian samples


ClinVar
Risk rs1006615(A,T;A,T)
Alt rs1006615(A,T;A,T)
Reference rs1006615(C;C)
Significance Untested
Disease Malignant melanoma
Variation info
Gene HMCN2
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000009.12:g.130433393C>A
CLNSRC ClinVar
CLNACC RCV000068558.1,