rs515726190

Orientation

plus

Stabilized

plus

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

Make rs515726190(C;C)

Make rs515726190(C;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102218942

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726190
dbSNP (classic)	rs515726190
ClinGen	rs515726190
ebi	rs515726190
HLI	rs515726190
Exac	rs515726190
Gnomad	rs515726190
Varsome	rs515726190
LitVar	rs515726190
Map	rs515726190
PheGenI	rs515726190
Biobank	rs515726190
1000 genomes	rs515726190
hgdp	rs515726190
ensembl	rs515726190
geneview	rs515726190
scholar	rs515726190
google	rs515726190
pharmgkb	rs515726190
gwascentral	rs515726190
openSNP	rs515726190
23andMe	rs515726190
SNPshot	rs515726190
SNPdbe	rs515726190
MSV3d	rs515726190
GWAS Ctlg	rs515726190

Max Magnitude

0

ClinVar
Risk	rs515726190(C;C)
Alt	rs515726190(C;C)
Reference	Rs515726190(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.103231170T>C
CLNSRC	ClinVar
CLNACC	RCV000118998.2,