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rs199907548

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199907548(A;G)
Make rs199907548(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position21974682
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs199907548
ebirs199907548
HLIrs199907548
Exacrs199907548
Varsomers199907548
Maprs199907548
PheGenIrs199907548
hapmaprs199907548
1000 genomesrs199907548
hgdprs199907548
ensemblrs199907548
gopubmedrs199907548
geneviewrs199907548
scholarrs199907548
googlers199907548
pharmgkbrs199907548
gwascentralrs199907548
openSNPrs199907548
23andMers199907548
23andMe allrs199907548
SNP Nexus

SNPshotrs199907548
SNPdbers199907548
MSV3drs199907548
GWAS Ctlgrs199907548
Max Magnitude0
ClinVar
Risk rs199907548(G;G)
Alt rs199907548(G;G)
Reference rs199907548(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not specified
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not specified
Reversed 0
HGVS NC_000009.11:g.21974681A>G
CLNSRC
CLNACC RCV000115331.5, RCV000122945.4, RCV000212398.1,