rs878853122

Orientation

plus

Stabilized

plus

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

Make rs878853122(-;G)

Make rs878853122(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

72225019

Gene

INPPL1

is a	snp
is	mentioned by
dbSNP	rs878853122
dbSNP (classic)	rs878853122
ClinGen	rs878853122
ebi	rs878853122
HLI	rs878853122
Exac	rs878853122
Gnomad	rs878853122
Varsome	rs878853122
LitVar	rs878853122
Map	rs878853122
PheGenI	rs878853122
Biobank	rs878853122
1000 genomes	rs878853122
hgdp	rs878853122
ensembl	rs878853122
geneview	rs878853122
scholar	rs878853122
google	rs878853122
pharmgkb	rs878853122
gwascentral	rs878853122
openSNP	rs878853122
23andMe	rs878853122
SNPshot	rs878853122
SNPdbe	rs878853122
MSV3d	rs878853122
GWAS Ctlg	rs878853122

Max Magnitude

0

ClinVar
Risk	rs878853122(G;G)
Alt	rs878853122(G;G)
Reference	Rs878853122(-;-)
Significance	Pathogenic
Disease	Opsismodysplasia
Variation	info
Gene	INPPL1
CLNDBN	Opsismodysplasia
Reversed	0
HGVS	NC_000011.9:g.71936063dupG
CLNSRC
CLNACC	RCV000224773.1,