rs145632008

Orientation

plus

Stabilized

plus

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

Make rs145632008(C;T)

Make rs145632008(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

3417922

Gene

PRDM16

is a	snp
is	mentioned by
dbSNP	rs145632008
dbSNP (classic)	rs145632008
ClinGen	rs145632008
ebi	rs145632008
HLI	rs145632008
Exac	rs145632008
Gnomad	rs145632008
Varsome	rs145632008
LitVar	rs145632008
Map	rs145632008
PheGenI	rs145632008
Biobank	rs145632008
1000 genomes	rs145632008
hgdp	rs145632008
ensembl	rs145632008
geneview	rs145632008
scholar	rs145632008
google	rs145632008
pharmgkb	rs145632008
gwascentral	rs145632008
openSNP	rs145632008
23andMe	rs145632008
SNPshot	rs145632008
SNPdbe	rs145632008
MSV3d	rs145632008
GWAS Ctlg	rs145632008

Max Magnitude

0

ClinVar
Risk	rs145632008(A;A) rs145632008(T;T)
Alt	rs145632008(A;A) rs145632008(T;T)
Reference	Rs145632008(C;C)
Significance	Untested
Disease	not specified
Variation	info
Gene	PRDM16
CLNDBN	not specified
Reversed	0
HGVS	NC_000001.10:g.3334486C>A
CLNSRC	ClinVar
CLNACC	RCV000219521.1,

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