rs515726187

Orientation

plus

Stabilized

plus

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

Make rs515726187(A;G)

Make rs515726187(G;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102224972

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726187
dbSNP (classic)	rs515726187
ClinGen	rs515726187
ebi	rs515726187
HLI	rs515726187
Exac	rs515726187
Gnomad	rs515726187
Varsome	rs515726187
LitVar	rs515726187
Map	rs515726187
PheGenI	rs515726187
Biobank	rs515726187
1000 genomes	rs515726187
hgdp	rs515726187
ensembl	rs515726187
geneview	rs515726187
scholar	rs515726187
google	rs515726187
pharmgkb	rs515726187
gwascentral	rs515726187
openSNP	rs515726187
23andMe	rs515726187
SNPshot	rs515726187
SNPdbe	rs515726187
MSV3d	rs515726187
GWAS Ctlg	rs515726187

Max Magnitude

0

ClinVar
Risk	rs515726187(G;G)
Alt	rs515726187(G;G)
Reference	Rs515726187(A;A)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103237200A>G
CLNSRC	ClinVar
CLNACC	RCV000118995.2,