rs78705382

Orientation

plus

Stabilized

plus

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

Make rs78705382(C;T)

Make rs78705382(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

50934975

Gene

RNASEH2B

is a	snp
is	mentioned by
dbSNP	rs78705382
dbSNP (classic)	rs78705382
ClinGen	rs78705382
ebi	rs78705382
HLI	rs78705382
Exac	rs78705382
Gnomad	rs78705382
Varsome	rs78705382
LitVar	rs78705382
Map	rs78705382
PheGenI	rs78705382
Biobank	rs78705382
1000 genomes	rs78705382
hgdp	rs78705382
ensembl	rs78705382
geneview	rs78705382
scholar	rs78705382
google	rs78705382
pharmgkb	rs78705382
gwascentral	rs78705382
openSNP	rs78705382
23andMe	rs78705382
SNPshot	rs78705382
SNPdbe	rs78705382
MSV3d	rs78705382
GWAS Ctlg	rs78705382

Max Magnitude

0

ClinVar
Risk	rs78705382(T;T)
Alt	rs78705382(T;T)
Reference	Rs78705382(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RNASEH2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.51509111C>T
CLNSRC
CLNACC	RCV000412805.1,