rs193922335

Orientation

minus

Stabilized

minus

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

Make rs193922335(A;T)

Make rs193922335(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44146611

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922335
dbSNP (classic)	rs193922335
ClinGen	rs193922335
ebi	rs193922335
HLI	rs193922335
Exac	rs193922335
Gnomad	rs193922335
Varsome	rs193922335
LitVar	rs193922335
Map	rs193922335
PheGenI	rs193922335
Biobank	rs193922335
1000 genomes	rs193922335
hgdp	rs193922335
ensembl	rs193922335
geneview	rs193922335
scholar	rs193922335
google	rs193922335
pharmgkb	rs193922335
gwascentral	rs193922335
openSNP	rs193922335
23andMe	rs193922335
SNPshot	rs193922335
SNPdbe	rs193922335
MSV3d	rs193922335
GWAS Ctlg	rs193922335

Max Magnitude

0

ClinVar
Risk	rs193922335(G;G) rs193922335(T;T)
Alt	rs193922335(G;G) rs193922335(T;T)
Reference	Rs193922335(A;A)
Significance	Pathogenic
Disease	Maturity-onset diabetes of the young not provided
Variation	info
Gene	GCK
CLNDBN	Maturity-onset diabetes of the young, type 2 not provided
Reversed	1
HGVS	NC_000007.13:g.44186210T>A; NC_000007.13:g.44186210T>C
CLNSRC	ClinVar
CLNACC	RCV000029926.1, RCV000485201.1,