rs193922271

Orientation

minus

Stabilized

minus

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

Make rs193922271(C;G)

Make rs193922271(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145543

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922271
dbSNP (classic)	rs193922271
ClinGen	rs193922271
ebi	rs193922271
HLI	rs193922271
Exac	rs193922271
Gnomad	rs193922271
Varsome	rs193922271
LitVar	rs193922271
Map	rs193922271
PheGenI	rs193922271
Biobank	rs193922271
1000 genomes	rs193922271
hgdp	rs193922271
ensembl	rs193922271
geneview	rs193922271
scholar	rs193922271
google	rs193922271
pharmgkb	rs193922271
gwascentral	rs193922271
openSNP	rs193922271
23andMe	rs193922271
SNPshot	rs193922271
SNPdbe	rs193922271
MSV3d	rs193922271
GWAS Ctlg	rs193922271

Max Magnitude

0

ClinVar
Risk	rs193922271(A;A) rs193922271(G;G)
Alt	rs193922271(A;A) rs193922271(G;G)
Reference	Rs193922271(C;C)
Significance	Probable-Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	GCK
CLNDBN	Maturity-onset diabetes of the young, type 2
Reversed	1
HGVS	NC_000007.13:g.44185142G>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029850.1,