rs1057522775

Orientation

plus

Stabilized

plus

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

Make rs1057522775(C;C)

Make rs1057522775(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

69956457

Gene

MITF

is a	snp
is	mentioned by
dbSNP	rs1057522775
dbSNP (classic)	rs1057522775
ClinGen	rs1057522775
ebi	rs1057522775
HLI	rs1057522775
Exac	rs1057522775
Gnomad	rs1057522775
Varsome	rs1057522775
LitVar	rs1057522775
Map	rs1057522775
PheGenI	rs1057522775
Biobank	rs1057522775
1000 genomes	rs1057522775
hgdp	rs1057522775
ensembl	rs1057522775
geneview	rs1057522775
scholar	rs1057522775
google	rs1057522775
pharmgkb	rs1057522775
gwascentral	rs1057522775
openSNP	rs1057522775
23andMe	rs1057522775
SNPshot	rs1057522775
SNPdbe	rs1057522775
MSV3d	rs1057522775
GWAS Ctlg	rs1057522775

Max Magnitude

0

ClinVar
Risk	rs1057522775(C;C)
Alt	rs1057522775(C;C)
Reference	Rs1057522775(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MITF
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.70005608G>C
CLNSRC
CLNACC	RCV000424648.1,