rs730882162

Orientation

plus

Stabilized

plus

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

Make rs730882162(A;A)

Make rs730882162(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

232525249

Gene	CHRND, PRSS56

is a	snp
is	mentioned by
dbSNP	rs730882162
dbSNP (classic)	rs730882162
ClinGen	rs730882162
ebi	rs730882162
HLI	rs730882162
Exac	rs730882162
Gnomad	rs730882162
Varsome	rs730882162
LitVar	rs730882162
Map	rs730882162
PheGenI	rs730882162
Biobank	rs730882162
1000 genomes	rs730882162
hgdp	rs730882162
ensembl	rs730882162
geneview	rs730882162
scholar	rs730882162
google	rs730882162
pharmgkb	rs730882162
gwascentral	rs730882162
openSNP	rs730882162
23andMe	rs730882162
SNPshot	rs730882162
SNPdbe	rs730882162
MSV3d	rs730882162
GWAS Ctlg	rs730882162

Max Magnitude

0

ClinVar
Risk	rs730882162(A;A) rs730882162(C;C)
Alt	rs730882162(A;A) rs730882162(C;C)
Reference	Rs730882162(G;G)
Significance	Pathogenic
Disease	Microphthalmia
Variation	info
Gene	CHRND PRSS56
CLNDBN	Microphthalmia, isolated 6
Reversed	0
HGVS	NC_000002.11:g.233389959G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000162043.3,