rs137852674

Orientation

minus

Stabilized

minus

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

Make rs137852674(C;G)

Make rs137852674(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17430887

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs137852674
dbSNP (classic)	rs137852674
ClinGen	rs137852674
ebi	rs137852674
HLI	rs137852674
Exac	rs137852674
Gnomad	rs137852674
Varsome	rs137852674
LitVar	rs137852674
Map	rs137852674
PheGenI	rs137852674
Biobank	rs137852674
1000 genomes	rs137852674
hgdp	rs137852674
ensembl	rs137852674
geneview	rs137852674
scholar	rs137852674
google	rs137852674
pharmgkb	rs137852674
gwascentral	rs137852674
openSNP	rs137852674
23andMe	rs137852674
SNPshot	rs137852674
SNPdbe	rs137852674
MSV3d	rs137852674
GWAS Ctlg	rs137852674

Max Magnitude

0

OMIM	600509
Desc
Variant	0020
Related	also

ClinVar
Risk	rs137852674(G;G)
Alt	rs137852674(G;G)
Reference	Rs137852674(C;C)
Significance	Pathogenic
Disease	Transient neonatal diabetes mellitus 2 Diabetes mellitus type 2
Variation	info
Gene	ABCC8
CLNDBN	Transient neonatal diabetes mellitus 2 Diabetes mellitus type 2
Reversed	1
HGVS	NC_000011.9:g.17452434G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009675.3, RCV000009676.3,