rs387906538

Orientation

minus

Stabilized

minus

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

Make rs387906538(C;T)

Make rs387906538(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7132230

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs387906538
dbSNP (classic)	rs387906538
ClinGen	rs387906538
ebi	rs387906538
HLI	rs387906538
Exac	rs387906538
Gnomad	rs387906538
Varsome	rs387906538
LitVar	rs387906538
Map	rs387906538
PheGenI	rs387906538
Biobank	rs387906538
1000 genomes	rs387906538
hgdp	rs387906538
ensembl	rs387906538
geneview	rs387906538
scholar	rs387906538
google	rs387906538
pharmgkb	rs387906538
gwascentral	rs387906538
openSNP	rs387906538
23andMe	rs387906538
SNPshot	rs387906538
SNPdbe	rs387906538
MSV3d	rs387906538
GWAS Ctlg	rs387906538

Max Magnitude

0

ClinVar
Risk	rs387906538(G;G) rs387906538(T;T)
Alt	rs387906538(G;G) rs387906538(T;T)
Reference	Rs387906538(C;C)
Significance	Pathogenic
Disease	Leprechaunism syndrome
Variation	info
Gene	INSR
CLNDBN	Leprechaunism syndrome
Reversed	1
HGVS	NC_000019.9:g.7132241G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015800.30,