rs515726198

Orientation

plus

Stabilized

plus

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

Make rs515726198(A;C)

Make rs515726198(C;C)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102208240

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726198
dbSNP (classic)	rs515726198
ClinGen	rs515726198
ebi	rs515726198
HLI	rs515726198
Exac	rs515726198
Gnomad	rs515726198
Varsome	rs515726198
LitVar	rs515726198
Map	rs515726198
PheGenI	rs515726198
Biobank	rs515726198
1000 genomes	rs515726198
hgdp	rs515726198
ensembl	rs515726198
geneview	rs515726198
scholar	rs515726198
google	rs515726198
pharmgkb	rs515726198
gwascentral	rs515726198
openSNP	rs515726198
23andMe	rs515726198
SNPshot	rs515726198
SNPdbe	rs515726198
MSV3d	rs515726198
GWAS Ctlg	rs515726198

Max Magnitude

0

ClinVar
Risk	rs515726198(C;C)
Alt	rs515726198(C;C)
Reference	Rs515726198(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.103220468A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000119012.2,