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rs1060501265

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060501265(C;C)
Make rs1060501265(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21974676
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs1060501265
dbSNP (old)rs1060501265
ClinGenrs1060501265
ebirs1060501265
HLIrs1060501265
Exacrs1060501265
Gnomadrs1060501265
Varsomers1060501265
LitVarrs1060501265
Maprs1060501265
PheGenIrs1060501265
Biobankrs1060501265
1000 genomesrs1060501265
hgdprs1060501265
ensemblrs1060501265
gopubmedrs1060501265
geneviewrs1060501265
scholarrs1060501265
googlers1060501265
pharmgkbrs1060501265
gwascentralrs1060501265
openSNPrs1060501265
23andMers1060501265
23andMe allrs1060501265
SNPshotrs1060501265
SNPdbers1060501265
MSV3drs1060501265
GWAS Ctlgrs1060501265
Max Magnitude0
ClinVar
Risk rs1060501265(C;C)
Alt rs1060501265(C;C)
Reference Rs1060501265(T;T)
Significance Probable-Pathogenic
Disease Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21974675A>G
CLNSRC
CLNACC RCV000459258.1,