rs397507523

Orientation

plus

Stabilized

plus

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

Make rs397507523(A;G)

Make rs397507523(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

112472954

Gene

PTPN11

is a	snp
is	mentioned by
dbSNP	rs397507523
dbSNP (classic)	rs397507523
ClinGen	rs397507523
ebi	rs397507523
HLI	rs397507523
Exac	rs397507523
Gnomad	rs397507523
Varsome	rs397507523
LitVar	rs397507523
Map	rs397507523
PheGenI	rs397507523
Biobank	rs397507523
1000 genomes	rs397507523
hgdp	rs397507523
ensembl	rs397507523
geneview	rs397507523
scholar	rs397507523
google	rs397507523
pharmgkb	rs397507523
gwascentral	rs397507523
openSNP	rs397507523
23andMe	rs397507523
SNPshot	rs397507523
SNPdbe	rs397507523
MSV3d	rs397507523
GWAS Ctlg	rs397507523

Max Magnitude

0

ClinVar
Risk	rs397507523(G;G)
Alt	rs397507523(G;G)
Reference	Rs397507523(A;A)
Significance	Other
Disease	Rasopathy not provided
Variation	info
Gene	PTPN11
CLNDBN	Rasopathy not provided
Reversed	0
HGVS	NC_000012.11:g.112910758A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000033497.6, RCV000157681.2,