rs397507508

Orientation

plus

Stabilized

plus

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

Make rs397507508(GTGA;T)

Make rs397507508(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

112450359

Gene

PTPN11

is a	snp
is	mentioned by
dbSNP	rs397507508
dbSNP (classic)	rs397507508
ClinGen	rs397507508
ebi	rs397507508
HLI	rs397507508
Exac	rs397507508
Gnomad	rs397507508
Varsome	rs397507508
LitVar	rs397507508
Map	rs397507508
PheGenI	rs397507508
Biobank	rs397507508
1000 genomes	rs397507508
hgdp	rs397507508
ensembl	rs397507508
geneview	rs397507508
scholar	rs397507508
google	rs397507508
pharmgkb	rs397507508
gwascentral	rs397507508
openSNP	rs397507508
23andMe	rs397507508
SNPshot	rs397507508
SNPdbe	rs397507508
MSV3d	rs397507508
GWAS Ctlg	rs397507508

Max Magnitude

0

ClinVar
Risk	rs397507508(T;T)
Alt	rs397507508(T;T)
Reference	Rs397507508(GTGA;GTGA)
Significance	Pathogenic
Disease	Rasopathy
Variation	info
Gene	PTPN11
CLNDBN	Rasopathy
Reversed	0
HGVS	NC_000012.11:g.112888163_112888166delGTGAinsT
CLNSRC	ClinVar
CLNACC	RCV000033460.2,