rs886037955

Orientation

plus

Stabilized

plus

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

Make rs886037955(A;A)

Make rs886037955(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

28793938

Gene

PPP1CB

is a	snp
is	mentioned by
dbSNP	rs886037955
dbSNP (classic)	rs886037955
ClinGen	rs886037955
ebi	rs886037955
HLI	rs886037955
Exac	rs886037955
Gnomad	rs886037955
Varsome	rs886037955
LitVar	rs886037955
Map	rs886037955
PheGenI	rs886037955
Biobank	rs886037955
1000 genomes	rs886037955
hgdp	rs886037955
ensembl	rs886037955
geneview	rs886037955
scholar	rs886037955
google	rs886037955
pharmgkb	rs886037955
gwascentral	rs886037955
openSNP	rs886037955
23andMe	rs886037955
SNPshot	rs886037955
SNPdbe	rs886037955
MSV3d	rs886037955
GWAS Ctlg	rs886037955

Max Magnitude

0

ClinVar
Risk	rs886037955(A;A)
Alt	rs886037955(A;A)
Reference	Rs886037955(G;G)
Significance	Pathogenic
Disease	not provided Noonan syndrome-like disorder with loose anagen hair 2
Variation	info
Gene	PPP1CB
CLNDBN	not provided Noonan syndrome-like disorder with loose anagen hair 2
Reversed	0
HGVS	NC_000002.11:g.29016804G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000257961.1, RCV000490625.1,