rs372670098

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs372670098(C;C)

Make rs372670098(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

21971153

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs372670098
dbSNP (classic)	rs372670098
ClinGen	rs372670098
ebi	rs372670098
HLI	rs372670098
Exac	rs372670098
Gnomad	rs372670098
Varsome	rs372670098
LitVar	rs372670098
Map	rs372670098
PheGenI	rs372670098
Biobank	rs372670098
1000 genomes	rs372670098
hgdp	rs372670098
ensembl	rs372670098
geneview	rs372670098
scholar	rs372670098
google	rs372670098
pharmgkb	rs372670098
gwascentral	rs372670098
openSNP	rs372670098
23andMe	rs372670098
SNPshot	rs372670098
SNPdbe	rs372670098
MSV3d	rs372670098
GWAS Ctlg	rs372670098

Max Magnitude

0

ClinVar
Risk	rs372670098(C;C)
Alt	rs372670098(C;C)
Reference	Rs372670098(T;T)
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.21971152T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000166237.3, RCV000205699.1, RCV000235616.2,