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rs11552822

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11552822(G;T)
Make rs11552822(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position21971109
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs11552822
dbSNP (old)rs11552822
ClinGenrs11552822
ebirs11552822
HLIrs11552822
Exacrs11552822
Gnomadrs11552822
Varsomers11552822
Maprs11552822
PheGenIrs11552822
Biobankrs11552822
1000 genomesrs11552822
hgdprs11552822
ensemblrs11552822
gopubmedrs11552822
geneviewrs11552822
scholarrs11552822
googlers11552822
pharmgkbrs11552822
gwascentralrs11552822
openSNPrs11552822
23andMers11552822
23andMe allrs11552822
SNPshotrs11552822
SNPdbers11552822
MSV3drs11552822
GWAS Ctlgrs11552822
Max Magnitude0
ClinVar
Risk rs11552822(A;A) rs11552822(T;T)
Alt rs11552822(A;A) rs11552822(T;T)
Reference Rs11552822(G;G)
Significance Probable-Pathogenic
Disease Neoplasm Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma
Variation info
Gene CDKN2A
CLNDBN Neoplasm Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma
Reversed 1
HGVS NC_000009.11:g.21971108C>A; NC_000009.11:g.21971108C>T
CLNSRC
CLNACC RCV000419046.1, RCV000214736.1, RCV000474240.1,