rs121918101

Orientation

minus

Stabilized

minus

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

Make rs121918101(C;G)

Make rs121918101(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2160872

Gene	INS, INS-IGF2

is a	snp
is	mentioned by
dbSNP	rs121918101
dbSNP (classic)	rs121918101
ClinGen	rs121918101
ebi	rs121918101
HLI	rs121918101
Exac	rs121918101
Gnomad	rs121918101
Varsome	rs121918101
LitVar	rs121918101
Map	rs121918101
PheGenI	rs121918101
Biobank	rs121918101
1000 genomes	rs121918101
hgdp	rs121918101
ensembl	rs121918101
geneview	rs121918101
scholar	rs121918101
google	rs121918101
pharmgkb	rs121918101
gwascentral	rs121918101
openSNP	rs121918101
23andMe	rs121918101
SNPshot	rs121918101
SNPdbe	rs121918101
MSV3d	rs121918101
GWAS Ctlg	rs121918101

Max Magnitude

0

OMIM	176730
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918101(G;G)
Alt	rs121918101(G;G)
Reference	Rs121918101(C;C)
Significance	Pathogenic
Disease	Hyperproinsulinemia
Variation	info
Gene	INS INS-IGF2
CLNDBN	Hyperproinsulinemia
Reversed	1
HGVS	NC_000011.9:g.2182102G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014308.26,