rs1057518878

Orientation

minus

Stabilized

minus

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

Make rs1057518878(C;G)

Make rs1057518878(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

79599715

Gene	LOC101928230, MAF

is a	snp
is	mentioned by
dbSNP	rs1057518878
dbSNP (classic)	rs1057518878
ClinGen	rs1057518878
ebi	rs1057518878
HLI	rs1057518878
Exac	rs1057518878
Gnomad	rs1057518878
Varsome	rs1057518878
LitVar	rs1057518878
Map	rs1057518878
PheGenI	rs1057518878
Biobank	rs1057518878
1000 genomes	rs1057518878
hgdp	rs1057518878
ensembl	rs1057518878
geneview	rs1057518878
scholar	rs1057518878
google	rs1057518878
pharmgkb	rs1057518878
gwascentral	rs1057518878
openSNP	rs1057518878
23andMe	rs1057518878
SNPshot	rs1057518878
SNPdbe	rs1057518878
MSV3d	rs1057518878
GWAS Ctlg	rs1057518878

Max Magnitude

0

ClinVar
Risk	rs1057518878(G;G)
Alt	rs1057518878(G;G)
Reference	Rs1057518878(C;C)
Significance	Probable-Pathogenic
Disease	Congenital cataract
Variation	info
Gene	MAF LOC101928230
CLNDBN	Congenital cataract
Reversed	1
HGVS	NC_000016.9:g.79633612G>C
CLNSRC
CLNACC	RCV000415117.1,