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rs137854599

From SNPedia

Orientationminus
Stabilizedminus
Make rs137854599(A;A)
Make rs137854599(A;G)
Make rs137854599(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position21971093
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs137854599
dbSNP (old)rs137854599
ClinGenrs137854599
ebirs137854599
HLIrs137854599
Exacrs137854599
Varsomers137854599
Maprs137854599
PheGenIrs137854599
Biobankrs137854599
1000 genomesrs137854599
hgdprs137854599
ensemblrs137854599
gopubmedrs137854599
geneviewrs137854599
scholarrs137854599
googlers137854599
pharmgkbrs137854599
gwascentralrs137854599
openSNPrs137854599
23andMers137854599
23andMe allrs137854599
SNP Nexus

SNPshotrs137854599
SNPdbers137854599
MSV3drs137854599
GWAS Ctlgrs137854599
Max Magnitude
OMIM600160
Desc
Variant0019
Relatedalso
ClinVar
Risk rs137854599(A;A)
Alt rs137854599(A;A)
Reference rs137854599(G;G)
Significance Other
Disease Melanoma Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome not provided
Variation info
Gene CDKN2A
CLNDBN Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000009.11:g.21971092C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000010033.2, RCV000122946.1, RCV000219725.2, RCV000493646.1,