rs397515467

Orientation

minus

Stabilized

minus

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

Make rs397515467(G;T)

Make rs397515467(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

77322434

Gene

ADAMTS18

is a	snp
is	mentioned by
dbSNP	rs397515467
dbSNP (classic)	rs397515467
ClinGen	rs397515467
ebi	rs397515467
HLI	rs397515467
Exac	rs397515467
Gnomad	rs397515467
Varsome	rs397515467
LitVar	rs397515467
Map	rs397515467
PheGenI	rs397515467
Biobank	rs397515467
1000 genomes	rs397515467
hgdp	rs397515467
ensembl	rs397515467
geneview	rs397515467
scholar	rs397515467
google	rs397515467
pharmgkb	rs397515467
gwascentral	rs397515467
openSNP	rs397515467
23andMe	rs397515467
SNPshot	rs397515467
SNPdbe	rs397515467
MSV3d	rs397515467
GWAS Ctlg	rs397515467

Max Magnitude

0

ClinVar
Risk	rs397515467(A;A) rs397515467(T;T)
Alt	rs397515467(A;A) rs397515467(T;T)
Reference	Rs397515467(G;G)
Significance	Pathogenic
Disease	Microcornea
Variation	info
Gene	ADAMTS18
CLNDBN	Microcornea, myopic chorioretinal atrophy, and telecanthus
Reversed	1
HGVS	NC_000016.9:g.77356331C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000056279.2,