rs193921340

Orientation

minus

Stabilized

minus

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

Make rs193921340(A;A)

Make rs193921340(A;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145581

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193921340
dbSNP (classic)	rs193921340
ClinGen	rs193921340
ebi	rs193921340
HLI	rs193921340
Exac	rs193921340
Gnomad	rs193921340
Varsome	rs193921340
LitVar	rs193921340
Map	rs193921340
PheGenI	rs193921340
Biobank	rs193921340
1000 genomes	rs193921340
hgdp	rs193921340
ensembl	rs193921340
geneview	rs193921340
scholar	rs193921340
google	rs193921340
pharmgkb	rs193921340
gwascentral	rs193921340
openSNP	rs193921340
23andMe	rs193921340
SNPshot	rs193921340
SNPdbe	rs193921340
MSV3d	rs193921340
GWAS Ctlg	rs193921340

Max Magnitude

0

ClinVar
Risk	rs193921340(A;A) rs193921340(C;C)
Alt	rs193921340(A;A) rs193921340(C;C)
Reference	Rs193921340(T;T)
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.44185180A>G; NC_000007.13:g.44185180A>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029847.1, RCV000029846.1,