rs515726191

Orientation

plus

Stabilized

plus

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

Make rs515726191(C;C)

Make rs515726191(C;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102218917

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726191
dbSNP (classic)	rs515726191
ClinGen	rs515726191
ebi	rs515726191
HLI	rs515726191
Exac	rs515726191
Gnomad	rs515726191
Varsome	rs515726191
LitVar	rs515726191
Map	rs515726191
PheGenI	rs515726191
Biobank	rs515726191
1000 genomes	rs515726191
hgdp	rs515726191
ensembl	rs515726191
geneview	rs515726191
scholar	rs515726191
google	rs515726191
pharmgkb	rs515726191
gwascentral	rs515726191
openSNP	rs515726191
23andMe	rs515726191
SNPshot	rs515726191
SNPdbe	rs515726191
MSV3d	rs515726191
GWAS Ctlg	rs515726191

Max Magnitude

0

ClinVar
Risk	rs515726191(C;C)
Alt	rs515726191(C;C)
Reference	Rs515726191(T;T)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103231145T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000119000.2,