rs193922396

Orientation

minus

Stabilized

minus

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

Make rs193922396(C;C)

Make rs193922396(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17442744

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs193922396
dbSNP (classic)	rs193922396
ClinGen	rs193922396
ebi	rs193922396
HLI	rs193922396
Exac	rs193922396
Gnomad	rs193922396
Varsome	rs193922396
LitVar	rs193922396
Map	rs193922396
PheGenI	rs193922396
Biobank	rs193922396
1000 genomes	rs193922396
hgdp	rs193922396
ensembl	rs193922396
geneview	rs193922396
scholar	rs193922396
google	rs193922396
pharmgkb	rs193922396
gwascentral	rs193922396
openSNP	rs193922396
23andMe	rs193922396
SNPshot	rs193922396
SNPdbe	rs193922396
MSV3d	rs193922396
GWAS Ctlg	rs193922396

Max Magnitude

0

ClinVar
Risk	rs193922396(C;C)
Alt	rs193922396(C;C)
Reference	Rs193922396(T;T)
Significance	Probable-Pathogenic
Disease	Neonatal diabetes mellitus
Variation	info
Gene	ABCC8
CLNDBN	Neonatal diabetes mellitus
Reversed	1
HGVS	NC_000011.9:g.17464291A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029251.1,