rs539275646

Orientation

plus

Stabilized

plus

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

Make rs539275646(C;T)

Make rs539275646(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

144055135

Gene

OPLAH

is a	snp
is	mentioned by
dbSNP	rs539275646
dbSNP (classic)	rs539275646
ClinGen	rs539275646
ebi	rs539275646
HLI	rs539275646
Exac	rs539275646
Gnomad	rs539275646
Varsome	rs539275646
LitVar	rs539275646
Map	rs539275646
PheGenI	rs539275646
Biobank	rs539275646
1000 genomes	rs539275646
hgdp	rs539275646
ensembl	rs539275646
geneview	rs539275646
scholar	rs539275646
google	rs539275646
pharmgkb	rs539275646
gwascentral	rs539275646
openSNP	rs539275646
23andMe	rs539275646
SNPshot	rs539275646
SNPdbe	rs539275646
MSV3d	rs539275646
GWAS Ctlg	rs539275646

Max Magnitude

0

ClinVar
Risk	rs539275646(T;T)
Alt	rs539275646(T;T)
Reference	Rs539275646(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	OPLAH
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.145110038C>T
CLNSRC
CLNACC	RCV000171537.1,