rs139901107

Orientation

plus

Stabilized

plus

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

Make rs139901107(A;A)

Make rs139901107(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

3839017

Gene

CEP104

is a	snp
is	mentioned by
dbSNP	rs139901107
dbSNP (classic)	rs139901107
ClinGen	rs139901107
ebi	rs139901107
HLI	rs139901107
Exac	rs139901107
Gnomad	rs139901107
Varsome	rs139901107
LitVar	rs139901107
Map	rs139901107
PheGenI	rs139901107
Biobank	rs139901107
1000 genomes	rs139901107
hgdp	rs139901107
ensembl	rs139901107
geneview	rs139901107
scholar	rs139901107
google	rs139901107
pharmgkb	rs139901107
gwascentral	rs139901107
openSNP	rs139901107
23andMe	rs139901107
SNPshot	rs139901107
SNPdbe	rs139901107
MSV3d	rs139901107
GWAS Ctlg	rs139901107

Max Magnitude

0

ClinVar
Risk	rs139901107(A;A)
Alt	rs139901107(A;A)
Reference	Rs139901107(G;G)
Significance	Untested
Disease	Malignant melanoma
Variation	info
Gene	CEP104
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000001.11:g.3839017G>A
CLNSRC	ClinVar
CLNACC	RCV000060189.2,

[PMID 21499247] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.