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rs33932559

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs33932559(C;C)
Make rs33932559(C;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position89919617
GeneMC1R
is asnp
is mentioned by
dbSNPrs33932559
dbSNP (old)rs33932559
ClinGenrs33932559
ebirs33932559
HLIrs33932559
Exacrs33932559
Varsomers33932559
Maprs33932559
PheGenIrs33932559
Biobankrs33932559
1000 genomesrs33932559
hgdprs33932559
ensemblrs33932559
gopubmedrs33932559
geneviewrs33932559
scholarrs33932559
googlers33932559
pharmgkbrs33932559
gwascentralrs33932559
openSNPrs33932559
23andMers33932559
23andMe allrs33932559
SNP Nexus

SNPshotrs33932559
SNPdbers33932559
MSV3drs33932559
GWAS Ctlgrs33932559
GMAF0.01561
Max Magnitude0

[PMID 23744330] [Association study of MC1R gene polymorphisms with freckles in Chinese Han population from Chengdu]

ClinVar
Risk rs33932559(C;C)
Alt rs33932559(C;C)
Reference Rs33932559(T;T)
Significance Probable-non-pathogenic
Disease not specified Malignant Melanoma Susceptibility Cutaneous malignant melanoma 5
Variation info
Gene MC1R
CLNDBN not specified Malignant Melanoma Susceptibility Cutaneous malignant melanoma 5
Reversed 0
HGVS NC_000016.9:g.89986025T>C
CLNSRC
CLNACC RCV000252453.1, RCV000339051.1, RCV000490361.1,