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rs1110400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1110400(C;C)
Make rs1110400(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89919722
GeneMC1R
is asnp
is mentioned by
dbSNPrs1110400
ClinGenrs1110400
ebirs1110400
HLIrs1110400
Exacrs1110400
Varsomers1110400
Maprs1110400
PheGenIrs1110400
hapmaprs1110400
1000 genomesrs1110400
hgdprs1110400
ensemblrs1110400
gopubmedrs1110400
geneviewrs1110400
scholarrs1110400
googlers1110400
pharmgkbrs1110400
gwascentralrs1110400
openSNPrs1110400
23andMers1110400
23andMe allrs1110400
SNP Nexus

SNPshotrs1110400
SNPdbers1110400
MSV3drs1110400
GWAS Ctlgrs1110400
Max Magnitude0
ClinVar
Risk rs1110400(C;C)
Alt rs1110400(C;C)
Reference Rs1110400(T;T)
Significance Pathogenic
Disease Cutaneous malignant melanoma 5 not specified not provided Malignant Melanoma Susceptibility
Variation info
Gene MC1R
CLNDBN Cutaneous malignant melanoma 5 not specified not provided Malignant Melanoma Susceptibility
Reversed 0
HGVS NC_000016.9:g.89986130T>C
CLNSRC Illumina
CLNACC RCV000230390.2, RCV000247792.1, RCV000254880.1, RCV000395366.1,