rs398124239

Orientation

plus

Stabilized

plus

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

Make rs398124239(-;-)

Make rs398124239(-;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

46854004

Gene

RP2

is a	snp
is	mentioned by
dbSNP	rs398124239
dbSNP (classic)	rs398124239
ClinGen	rs398124239
ebi	rs398124239
HLI	rs398124239
Exac	rs398124239
Gnomad	rs398124239
Varsome	rs398124239
LitVar	rs398124239
Map	rs398124239
PheGenI	rs398124239
Biobank	rs398124239
1000 genomes	rs398124239
hgdp	rs398124239
ensembl	rs398124239
geneview	rs398124239
scholar	rs398124239
google	rs398124239
pharmgkb	rs398124239
gwascentral	rs398124239
openSNP	rs398124239
23andMe	rs398124239
SNPshot	rs398124239
SNPdbe	rs398124239
MSV3d	rs398124239
GWAS Ctlg	rs398124239

Max Magnitude

0

ClinVar
Risk	rs398124239(-;-)
Alt	rs398124239(-;-)
Reference	Rs398124239(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.46713439delC
CLNSRC	ClinVar
CLNACC	RCV000081468.4,