rs121913155

Orientation

minus

Stabilized

minus

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

Make rs121913155(A;T)

Make rs121913155(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

7267555

Gene

INSR

is a	snp
is	mentioned by
dbSNP	rs121913155
dbSNP (classic)	rs121913155
ClinGen	rs121913155
ebi	rs121913155
HLI	rs121913155
Exac	rs121913155
Gnomad	rs121913155
Varsome	rs121913155
LitVar	rs121913155
Map	rs121913155
PheGenI	rs121913155
Biobank	rs121913155
1000 genomes	rs121913155
hgdp	rs121913155
ensembl	rs121913155
geneview	rs121913155
scholar	rs121913155
google	rs121913155
pharmgkb	rs121913155
gwascentral	rs121913155
openSNP	rs121913155
23andMe	rs121913155
SNPshot	rs121913155
SNPdbe	rs121913155
MSV3d	rs121913155
GWAS Ctlg	rs121913155

Max Magnitude

0

OMIM	147670
Desc
Variant	0027
Related	also

ClinVar
Risk	rs121913155(T;T)
Alt	rs121913155(T;T)
Reference	Rs121913155(A;A)
Significance	Pathogenic
Disease	Leprechaunism syndrome
Variation	info
Gene	INSR
CLNDBN	Leprechaunism syndrome
Reversed	1
HGVS	NC_000019.9:g.7267566T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015820.25,