rs587779350

Orientation

minus

Stabilized

minus

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

Make rs587779350(C;T)

Make rs587779350(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

102419619

Gene	IGF1, LOC105369942

is a	snp
is	mentioned by
dbSNP	rs587779350
dbSNP (classic)	rs587779350
ClinGen	rs587779350
ebi	rs587779350
HLI	rs587779350
Exac	rs587779350
Gnomad	rs587779350
Varsome	rs587779350
LitVar	rs587779350
Map	rs587779350
PheGenI	rs587779350
Biobank	rs587779350
1000 genomes	rs587779350
hgdp	rs587779350
ensembl	rs587779350
geneview	rs587779350
scholar	rs587779350
google	rs587779350
pharmgkb	rs587779350
gwascentral	rs587779350
openSNP	rs587779350
23andMe	rs587779350
SNPshot	rs587779350
SNPdbe	rs587779350
MSV3d	rs587779350
GWAS Ctlg	rs587779350

Max Magnitude

0

ClinVar
Risk	rs587779350(T;T)
Alt	rs587779350(T;T)
Reference	Rs587779350(C;C)
Significance	Pathogenic
Disease	Insulin-like growth factor I deficiency
Variation	info
Gene	IGF1
CLNDBN	Insulin-like growth factor I deficiency
Reversed	1
HGVS	NC_000012.11:g.102813397G>A
CLNSRC
CLNACC	RCV000115041.1,