rs397507521

Orientation

plus

Stabilized

plus

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

Make rs397507521(A;A)

Make rs397507521(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

112453317

Gene

PTPN11

is a	snp
is	mentioned by
dbSNP	rs397507521
dbSNP (classic)	rs397507521
ClinGen	rs397507521
ebi	rs397507521
HLI	rs397507521
Exac	rs397507521
Gnomad	rs397507521
Varsome	rs397507521
LitVar	rs397507521
Map	rs397507521
PheGenI	rs397507521
Biobank	rs397507521
1000 genomes	rs397507521
hgdp	rs397507521
ensembl	rs397507521
geneview	rs397507521
scholar	rs397507521
google	rs397507521
pharmgkb	rs397507521
gwascentral	rs397507521
openSNP	rs397507521
23andMe	rs397507521
SNPshot	rs397507521
SNPdbe	rs397507521
MSV3d	rs397507521
GWAS Ctlg	rs397507521

Max Magnitude

0

ClinVar
Risk	rs397507521(A;A)
Alt	rs397507521(A;A)
Reference	Rs397507521(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	PTPN11
CLNDBN	not provided not specified
Reversed	0
HGVS	NC_000012.11:g.112891121G>A
CLNSRC	ClinVar
CLNACC	RCV000033492.4, RCV000121913.1,