rs876661323

Orientation

plus

Stabilized

plus

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

Make rs876661323(-;G)

Make rs876661323(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

120955383

Gene

GLI2

is a	snp
is	mentioned by
dbSNP	rs876661323
dbSNP (classic)	rs876661323
ClinGen	rs876661323
ebi	rs876661323
HLI	rs876661323
Exac	rs876661323
Gnomad	rs876661323
Varsome	rs876661323
LitVar	rs876661323
Map	rs876661323
PheGenI	rs876661323
Biobank	rs876661323
1000 genomes	rs876661323
hgdp	rs876661323
ensembl	rs876661323
geneview	rs876661323
scholar	rs876661323
google	rs876661323
pharmgkb	rs876661323
gwascentral	rs876661323
openSNP	rs876661323
23andMe	rs876661323
SNPshot	rs876661323
SNPdbe	rs876661323
MSV3d	rs876661323
GWAS Ctlg	rs876661323

Max Magnitude

0

ClinVar
Risk	rs876661323(G;G)
Alt	rs876661323(G;G)
Reference	Rs876661323(-;-)
Significance	Probable-Pathogenic
Disease	microform holoprosencephaly
Variation	info
Gene	GLI2
CLNDBN	microform holoprosencephaly
Reversed	0
HGVS	NC_000002.11:g.121712959dupG
CLNSRC
CLNACC	RCV000223840.1,