rs1057520781

Orientation

plus

Stabilized

plus

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

Make rs1057520781(C;C)

Make rs1057520781(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

30668120

Gene

GK

is a	snp
is	mentioned by
dbSNP	rs1057520781
dbSNP (classic)	rs1057520781
ClinGen	rs1057520781
ebi	rs1057520781
HLI	rs1057520781
Exac	rs1057520781
Gnomad	rs1057520781
Varsome	rs1057520781
LitVar	rs1057520781
Map	rs1057520781
PheGenI	rs1057520781
Biobank	rs1057520781
1000 genomes	rs1057520781
hgdp	rs1057520781
ensembl	rs1057520781
geneview	rs1057520781
scholar	rs1057520781
google	rs1057520781
pharmgkb	rs1057520781
gwascentral	rs1057520781
openSNP	rs1057520781
23andMe	rs1057520781
SNPshot	rs1057520781
SNPdbe	rs1057520781
MSV3d	rs1057520781
GWAS Ctlg	rs1057520781

Max Magnitude

0

ClinVar
Risk	rs1057520781(C;C)
Alt	rs1057520781(C;C)
Reference	Rs1057520781(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GK
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.30686237T>C
CLNSRC
CLNACC	RCV000440001.1,