rs587782206

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;TGGC)	7	Pancreatic cancer/Melanoma Syndrome
(TGGC;TGGC)	0	common in clinvar

Make rs587782206(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

21974778

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs587782206
dbSNP (classic)	rs587782206
ClinGen	rs587782206
ebi	rs587782206
HLI	rs587782206
Exac	rs587782206
Gnomad	rs587782206
Varsome	rs587782206
LitVar	rs587782206
Map	rs587782206
PheGenI	rs587782206
Biobank	rs587782206
1000 genomes	rs587782206
hgdp	rs587782206
ensembl	rs587782206
geneview	rs587782206
scholar	rs587782206
google	rs587782206
pharmgkb	rs587782206
gwascentral	rs587782206
openSNP	rs587782206
23andMe	rs587782206
SNPshot	rs587782206
SNPdbe	rs587782206
MSV3d	rs587782206
GWAS Ctlg	rs587782206

Max Magnitude

7

ClinVar
Risk	rs587782206(-;-)
Alt	rs587782206(-;-)
Reference	Rs587782206(TGGC;TGGC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma
Variation	info
Gene	CDKN2A
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma
Reversed	1
HGVS	NC_000009.11:g.21974777_21974780delGCCA
CLNSRC
CLNACC	RCV000130872.3, RCV000458116.1,