rs61744404

Orientation

plus

Stabilized

plus

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

Make rs61744404(C;G)

Make rs61744404(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

232525489

Gene	CHRND, PRSS56

is a	snp
is	mentioned by
dbSNP	rs61744404
dbSNP (classic)	rs61744404
ClinGen	rs61744404
ebi	rs61744404
HLI	rs61744404
Exac	rs61744404
Gnomad	rs61744404
Varsome	rs61744404
LitVar	rs61744404
Map	rs61744404
PheGenI	rs61744404
Biobank	rs61744404
1000 genomes	rs61744404
hgdp	rs61744404
ensembl	rs61744404
geneview	rs61744404
scholar	rs61744404
google	rs61744404
pharmgkb	rs61744404
gwascentral	rs61744404
openSNP	rs61744404
23andMe	rs61744404
SNPshot	rs61744404
SNPdbe	rs61744404
MSV3d	rs61744404
GWAS Ctlg	rs61744404

GMAF

0.02342

Max Magnitude

0

ClinVar: benign

ClinVar
Risk	rs61744404(A;A) rs61744404(G;G)
Alt	rs61744404(A;A) rs61744404(G;G)
Reference	Rs61744404(C;C)
Significance	Non-pathogenic
Disease	Microphthalmia not specified
Variation	info
Gene	CHRND PRSS56
CLNDBN	Microphthalmia, isolated 6 not specified
Reversed	0
HGVS	NC_000002.11:g.233390199C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000024074.2, RCV000454640.1,