rs587777690

Orientation

plus

Stabilized

plus

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

Make rs587777690(C;C)

Make rs587777690(C;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

32940889

Gene

TMEM98

is a	snp
is	mentioned by
dbSNP	rs587777690
dbSNP (classic)	rs587777690
ClinGen	rs587777690
ebi	rs587777690
HLI	rs587777690
Exac	rs587777690
Gnomad	rs587777690
Varsome	rs587777690
LitVar	rs587777690
Map	rs587777690
PheGenI	rs587777690
Biobank	rs587777690
1000 genomes	rs587777690
hgdp	rs587777690
ensembl	rs587777690
geneview	rs587777690
scholar	rs587777690
google	rs587777690
pharmgkb	rs587777690
gwascentral	rs587777690
openSNP	rs587777690
23andMe	rs587777690
SNPshot	rs587777690
SNPdbe	rs587777690
MSV3d	rs587777690
GWAS Ctlg	rs587777690

Max Magnitude

0

ClinVar
Risk	rs587777690(C;C)
Alt	rs587777690(C;C)
Reference	Rs587777690(G;G)
Significance	Pathogenic
Disease	Nanophthalmos 4
Variation	info
Gene	TMEM98
CLNDBN	Nanophthalmos 4
Reversed	0
HGVS	NC_000017.10:g.31267907G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000143786.3,