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rs1060501266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060501266(A;G)
Make rs1060501266(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21968347
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs1060501266
dbSNP (classic)rs1060501266
ClinGenrs1060501266
ebirs1060501266
HLIrs1060501266
Exacrs1060501266
Gnomadrs1060501266
Varsomers1060501266
LitVarrs1060501266
Maprs1060501266
PheGenIrs1060501266
Biobankrs1060501266
1000 genomesrs1060501266
hgdprs1060501266
ensemblrs1060501266
geneviewrs1060501266
scholarrs1060501266
googlers1060501266
pharmgkbrs1060501266
gwascentralrs1060501266
openSNPrs1060501266
23andMers1060501266
SNPshotrs1060501266
SNPdbers1060501266
MSV3drs1060501266
GWAS Ctlgrs1060501266
Max Magnitude0
ClinVar
Risk rs1060501266(G;G)
Alt rs1060501266(G;G)
Reference Rs1060501266(A;A)
Significance Probable-Pathogenic
Disease Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21968346T>C
CLNSRC
CLNACC RCV000460188.1,