rs515726202

Orientation

plus

Stabilized

plus

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

Make rs515726202(C;C)

Make rs515726202(C;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102208143

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726202
dbSNP (classic)	rs515726202
ClinGen	rs515726202
ebi	rs515726202
HLI	rs515726202
Exac	rs515726202
Gnomad	rs515726202
Varsome	rs515726202
LitVar	rs515726202
Map	rs515726202
PheGenI	rs515726202
Biobank	rs515726202
1000 genomes	rs515726202
hgdp	rs515726202
ensembl	rs515726202
geneview	rs515726202
scholar	rs515726202
google	rs515726202
pharmgkb	rs515726202
gwascentral	rs515726202
openSNP	rs515726202
23andMe	rs515726202
SNPshot	rs515726202
SNPdbe	rs515726202
MSV3d	rs515726202
GWAS Ctlg	rs515726202

Max Magnitude

0

ClinVar
Risk	rs515726202(C;C)
Alt	rs515726202(C;C)
Reference	Rs515726202(G;G)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103220371G>C
CLNSRC	ClinVar
CLNACC	RCV000119017.2,