rs1057520647

Orientation

plus

Stabilized

plus

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

Make rs1057520647(C;T)

Make rs1057520647(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

30694499

Gene

GK

is a	snp
is	mentioned by
dbSNP	rs1057520647
dbSNP (classic)	rs1057520647
ClinGen	rs1057520647
ebi	rs1057520647
HLI	rs1057520647
Exac	rs1057520647
Gnomad	rs1057520647
Varsome	rs1057520647
LitVar	rs1057520647
Map	rs1057520647
PheGenI	rs1057520647
Biobank	rs1057520647
1000 genomes	rs1057520647
hgdp	rs1057520647
ensembl	rs1057520647
geneview	rs1057520647
scholar	rs1057520647
google	rs1057520647
pharmgkb	rs1057520647
gwascentral	rs1057520647
openSNP	rs1057520647
23andMe	rs1057520647
SNPshot	rs1057520647
SNPdbe	rs1057520647
MSV3d	rs1057520647
GWAS Ctlg	rs1057520647

Max Magnitude

0

ClinVar
Risk	rs1057520647(T;T)
Alt	rs1057520647(T;T)
Reference	Rs1057520647(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GK
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.30712616C>T
CLNSRC
CLNACC	RCV000433135.1,