rs193922406

Orientation

minus

Stabilized

minus

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

Make rs193922406(G;G)

Make rs193922406(G;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17393752

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs193922406
dbSNP (classic)	rs193922406
ClinGen	rs193922406
ebi	rs193922406
HLI	rs193922406
Exac	rs193922406
Gnomad	rs193922406
Varsome	rs193922406
LitVar	rs193922406
Map	rs193922406
PheGenI	rs193922406
Biobank	rs193922406
1000 genomes	rs193922406
hgdp	rs193922406
ensembl	rs193922406
geneview	rs193922406
scholar	rs193922406
google	rs193922406
pharmgkb	rs193922406
gwascentral	rs193922406
openSNP	rs193922406
23andMe	rs193922406
SNPshot	rs193922406
SNPdbe	rs193922406
MSV3d	rs193922406
GWAS Ctlg	rs193922406

Max Magnitude

0

ClinVar
Risk	rs193922406(G;G)
Alt	rs193922406(G;G)
Reference	Rs193922406(T;T)
Significance	Probable-Pathogenic
Disease	Neonatal diabetes mellitus
Variation	info
Gene	ABCC8
CLNDBN	Neonatal diabetes mellitus
Reversed	1
HGVS	NC_000011.9:g.17415299A>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029268.1,