rs515726200

Orientation

plus

Stabilized

plus

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

Make rs515726200(A;A)

Make rs515726200(A;C)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102208237

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726200
dbSNP (classic)	rs515726200
ClinGen	rs515726200
ebi	rs515726200
HLI	rs515726200
Exac	rs515726200
Gnomad	rs515726200
Varsome	rs515726200
LitVar	rs515726200
Map	rs515726200
PheGenI	rs515726200
Biobank	rs515726200
1000 genomes	rs515726200
hgdp	rs515726200
ensembl	rs515726200
geneview	rs515726200
scholar	rs515726200
google	rs515726200
pharmgkb	rs515726200
gwascentral	rs515726200
openSNP	rs515726200
23andMe	rs515726200
SNPshot	rs515726200
SNPdbe	rs515726200
MSV3d	rs515726200
GWAS Ctlg	rs515726200

Max Magnitude

0

ClinVar
Risk	rs515726200(A;A)
Alt	rs515726200(A;A)
Reference	Rs515726200(C;C)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103220465C>A
CLNSRC	ClinVar
CLNACC	RCV000119014.2,