rs515726195

Orientation

plus

Stabilized

plus

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

Make rs515726195(C;T)

Make rs515726195(T;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

102218866

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs515726195
dbSNP (classic)	rs515726195
ClinGen	rs515726195
ebi	rs515726195
HLI	rs515726195
Exac	rs515726195
Gnomad	rs515726195
Varsome	rs515726195
LitVar	rs515726195
Map	rs515726195
PheGenI	rs515726195
Biobank	rs515726195
1000 genomes	rs515726195
hgdp	rs515726195
ensembl	rs515726195
geneview	rs515726195
scholar	rs515726195
google	rs515726195
pharmgkb	rs515726195
gwascentral	rs515726195
openSNP	rs515726195
23andMe	rs515726195
SNPshot	rs515726195
SNPdbe	rs515726195
MSV3d	rs515726195
GWAS Ctlg	rs515726195

Max Magnitude

0

ClinVar
Risk	rs515726195(T;T)
Alt	rs515726195(T;T)
Reference	Rs515726195(C;C)
Significance	Pathogenic
Disease	RRM2B-related mitochondrial disease
Variation	info
Gene	RRM2B
CLNDBN	RRM2B-related mitochondrial disease
Reversed	0
HGVS	NC_000008.10:g.103231094C>T
CLNSRC	ClinVar
CLNACC	RCV000119004.2,