rs772913758

Orientation

plus

Stabilized

plus

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

Make rs772913758(C;C)

Make rs772913758(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

102238874

Gene	RRM2B, UBR5-AS1

is a	snp
is	mentioned by
dbSNP	rs772913758
dbSNP (classic)	rs772913758
ClinGen	rs772913758
ebi	rs772913758
HLI	rs772913758
Exac	rs772913758
Gnomad	rs772913758
Varsome	rs772913758
LitVar	rs772913758
Map	rs772913758
PheGenI	rs772913758
Biobank	rs772913758
1000 genomes	rs772913758
hgdp	rs772913758
ensembl	rs772913758
geneview	rs772913758
scholar	rs772913758
google	rs772913758
pharmgkb	rs772913758
gwascentral	rs772913758
openSNP	rs772913758
23andMe	rs772913758
SNPshot	rs772913758
SNPdbe	rs772913758
MSV3d	rs772913758
GWAS Ctlg	rs772913758

Max Magnitude

0

ClinVar
Risk	rs772913758(C;C)
Alt	rs772913758(C;C)
Reference	Rs772913758(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B LOC101927221 UBR5-AS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.103251102T>C
CLNSRC
CLNACC	RCV000493307.1,