rs397516811

Orientation

plus

Stabilized

plus

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

Make rs397516811(A;A)

Make rs397516811(A;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

112477655

Gene

PTPN11

is a	snp
is	mentioned by
dbSNP	rs397516811
dbSNP (classic)	rs397516811
ClinGen	rs397516811
ebi	rs397516811
HLI	rs397516811
Exac	rs397516811
Gnomad	rs397516811
Varsome	rs397516811
LitVar	rs397516811
Map	rs397516811
PheGenI	rs397516811
Biobank	rs397516811
1000 genomes	rs397516811
hgdp	rs397516811
ensembl	rs397516811
geneview	rs397516811
scholar	rs397516811
google	rs397516811
pharmgkb	rs397516811
gwascentral	rs397516811
openSNP	rs397516811
23andMe	rs397516811
SNPshot	rs397516811
SNPdbe	rs397516811
MSV3d	rs397516811
GWAS Ctlg	rs397516811

Max Magnitude

0

ClinVar
Risk	rs397516811(A;A)
Alt	rs397516811(A;A)
Reference	Rs397516811(T;T)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	PTPN11
CLNDBN	not specified
Reversed	0
HGVS	NC_000012.11:g.112915459T>A
CLNSRC	ClinVar
CLNACC	RCV000037666.3,