rs397507513

Orientation

plus

Stabilized

plus

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

Make rs397507513(A;C)

Make rs397507513(C;C)

Reference

GRCh38 38.1/141

Chromosome

12

Position

112450397

Gene

PTPN11

is a	snp
is	mentioned by
dbSNP	rs397507513
dbSNP (classic)	rs397507513
ClinGen	rs397507513
ebi	rs397507513
HLI	rs397507513
Exac	rs397507513
Gnomad	rs397507513
Varsome	rs397507513
LitVar	rs397507513
Map	rs397507513
PheGenI	rs397507513
Biobank	rs397507513
1000 genomes	rs397507513
hgdp	rs397507513
ensembl	rs397507513
geneview	rs397507513
scholar	rs397507513
google	rs397507513
pharmgkb	rs397507513
gwascentral	rs397507513
openSNP	rs397507513
23andMe	rs397507513
SNPshot	rs397507513
SNPdbe	rs397507513
MSV3d	rs397507513
GWAS Ctlg	rs397507513

Max Magnitude

0

ClinVar
Risk	rs397507513(C;C)
Alt	rs397507513(C;C)
Reference	Rs397507513(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PTPN11
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.112888201A>C
CLNSRC	ClinVar
CLNACC	RCV000033474.4,