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rs1060501263

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501263(-;-)
Make rs1060501263(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971001
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs1060501263
dbSNP (old)rs1060501263
ClinGenrs1060501263
ebirs1060501263
HLIrs1060501263
Exacrs1060501263
Gnomadrs1060501263
Varsomers1060501263
LitVarrs1060501263
Maprs1060501263
PheGenIrs1060501263
Biobankrs1060501263
1000 genomesrs1060501263
hgdprs1060501263
ensemblrs1060501263
gopubmedrs1060501263
geneviewrs1060501263
scholarrs1060501263
googlers1060501263
pharmgkbrs1060501263
gwascentralrs1060501263
openSNPrs1060501263
23andMers1060501263
23andMe allrs1060501263
SNPshotrs1060501263
SNPdbers1060501263
MSV3drs1060501263
GWAS Ctlgrs1060501263
Max Magnitude0
ClinVar
Risk rs1060501263(-;-)
Alt rs1060501263(-;-)
Reference Rs1060501263(G;G)
Significance Pathogenic
Disease Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21971000delC
CLNSRC
CLNACC RCV000465157.1,