rs145420390

Orientation

plus

Stabilized

plus

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

Make rs145420390(A;A)

Make rs145420390(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

3848618

Gene

CEP104

is a	snp
is	mentioned by
dbSNP	rs145420390
dbSNP (classic)	rs145420390
ClinGen	rs145420390
ebi	rs145420390
HLI	rs145420390
Exac	rs145420390
Gnomad	rs145420390
Varsome	rs145420390
LitVar	rs145420390
Map	rs145420390
PheGenI	rs145420390
Biobank	rs145420390
1000 genomes	rs145420390
hgdp	rs145420390
ensembl	rs145420390
geneview	rs145420390
scholar	rs145420390
google	rs145420390
pharmgkb	rs145420390
gwascentral	rs145420390
openSNP	rs145420390
23andMe	rs145420390
SNPshot	rs145420390
SNPdbe	rs145420390
MSV3d	rs145420390
GWAS Ctlg	rs145420390

Max Magnitude

0

ClinVar
Risk	rs145420390(A;A)
Alt	rs145420390(A;A)
Reference	Rs145420390(G;G)
Significance	Untested
Disease	Malignant melanoma
Variation	info
Gene	CEP104
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000001.11:g.3848618G>A
CLNSRC	ClinVar
CLNACC	RCV000060190.2,

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