rs397507507

Orientation

plus

Stabilized

plus

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

Make rs397507507(A;A)

Make rs397507507(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

112450358

Gene

PTPN11

is a	snp
is	mentioned by
dbSNP	rs397507507
dbSNP (classic)	rs397507507
ClinGen	rs397507507
ebi	rs397507507
HLI	rs397507507
Exac	rs397507507
Gnomad	rs397507507
Varsome	rs397507507
LitVar	rs397507507
Map	rs397507507
PheGenI	rs397507507
Biobank	rs397507507
1000 genomes	rs397507507
hgdp	rs397507507
ensembl	rs397507507
geneview	rs397507507
scholar	rs397507507
google	rs397507507
pharmgkb	rs397507507
gwascentral	rs397507507
openSNP	rs397507507
23andMe	rs397507507
SNPshot	rs397507507
SNPdbe	rs397507507
MSV3d	rs397507507
GWAS Ctlg	rs397507507

Max Magnitude

0

ClinVar
Risk	rs397507507(A;A) rs397507507(C;C) rs397507507(T;T)
Alt	rs397507507(A;A) rs397507507(C;C) rs397507507(T;T)
Reference	Rs397507507(G;G)
Significance	Other
Disease	Noonan syndrome not provided
Variation	info
Gene	PTPN11
CLNDBN	Noonan syndrome not provided
Reversed	0
HGVS	NC_000012.11:g.112888162G>A; NC_000012.11:g.112888162G>C; NC_000012.11:g.112888162G>T
CLNSRC	HGMD
CLNACC	RCV000151684.1, RCV000157700.2, RCV000413720.1, RCV000034327.6,