rs1057519616

Orientation

minus

Stabilized

minus

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

Make rs1057519616(-;C)

Make rs1057519616(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

56453607

Gene

MIP

is a	snp
is	mentioned by
dbSNP	rs1057519616
dbSNP (classic)	rs1057519616
ClinGen	rs1057519616
ebi	rs1057519616
HLI	rs1057519616
Exac	rs1057519616
Gnomad	rs1057519616
Varsome	rs1057519616
LitVar	rs1057519616
Map	rs1057519616
PheGenI	rs1057519616
Biobank	rs1057519616
1000 genomes	rs1057519616
hgdp	rs1057519616
ensembl	rs1057519616
geneview	rs1057519616
scholar	rs1057519616
google	rs1057519616
pharmgkb	rs1057519616
gwascentral	rs1057519616
openSNP	rs1057519616
23andMe	rs1057519616
SNPshot	rs1057519616
SNPdbe	rs1057519616
MSV3d	rs1057519616
GWAS Ctlg	rs1057519616

Max Magnitude

0

ClinVar
Risk	rs1057519616(C;C)
Alt	rs1057519616(C;C)
Reference	Rs1057519616(-;-)
Significance	Pathogenic
Disease	Cataract 15
Variation	info
Gene	MIP
CLNDBN	Cataract 15, multiple types
Reversed	1
HGVS	NC_000012.11:g.56847392dupG
CLNSRC
CLNACC	RCV000420543.1,