rs137854598

Orientation

minus

Stabilized

minus

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

Make rs137854598(A;A)

Make rs137854598(A;C)

Reference

GRCh38 38.1/141

Chromosome

9

Position

21971054

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs137854598
dbSNP (classic)	rs137854598
ClinGen	rs137854598
ebi	rs137854598
HLI	rs137854598
Exac	rs137854598
Gnomad	rs137854598
Varsome	rs137854598
LitVar	rs137854598
Map	rs137854598
PheGenI	rs137854598
Biobank	rs137854598
1000 genomes	rs137854598
hgdp	rs137854598
ensembl	rs137854598
geneview	rs137854598
scholar	rs137854598
google	rs137854598
pharmgkb	rs137854598
gwascentral	rs137854598
openSNP	rs137854598
23andMe	rs137854598
SNPshot	rs137854598
SNPdbe	rs137854598
MSV3d	rs137854598
GWAS Ctlg	rs137854598

Max Magnitude

0

OMIM	600160
Desc
Variant	0011
Related	also

ClinVar
Risk	rs137854598(A;A) rs137854598(T;T)
Alt	rs137854598(A;A) rs137854598(T;T)
Reference	Rs137854598(C;C)
Significance	Untested
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.21971053G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000220450.1, RCV000462689.1,