rs139934930

Orientation

plus

Stabilized

plus

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

Make rs139934930(C;T)

Make rs139934930(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

7827211

Gene

PER3

is a	snp
is	mentioned by
dbSNP	rs139934930
dbSNP (classic)	rs139934930
ClinGen	rs139934930
ebi	rs139934930
HLI	rs139934930
Exac	rs139934930
Gnomad	rs139934930
Varsome	rs139934930
LitVar	rs139934930
Map	rs139934930
PheGenI	rs139934930
Biobank	rs139934930
1000 genomes	rs139934930
hgdp	rs139934930
ensembl	rs139934930
geneview	rs139934930
scholar	rs139934930
google	rs139934930
pharmgkb	rs139934930
gwascentral	rs139934930
openSNP	rs139934930
23andMe	rs139934930
SNPshot	rs139934930
SNPdbe	rs139934930
MSV3d	rs139934930
GWAS Ctlg	rs139934930

Max Magnitude

0

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

ClinVar
Risk	rs139934930(T;T)
Alt	rs139934930(T;T)
Reference	Rs139934930(C;C)
Significance	Untested
Disease	Malignant melanoma
Variation	info
Gene	PER3
CLNDBN	Malignant melanoma
Reversed	0
HGVS	NC_000001.11:g.7827211C>T
CLNSRC	ClinVar
CLNACC	RCV000060248.2,