rs1057517815

Orientation

plus

Stabilized

plus

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

Make rs1057517815(A;G)

Make rs1057517815(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

50930675

Gene

RNASEH2B

is a	snp
is	mentioned by
dbSNP	rs1057517815
dbSNP (classic)	rs1057517815
ClinGen	rs1057517815
ebi	rs1057517815
HLI	rs1057517815
Exac	rs1057517815
Gnomad	rs1057517815
Varsome	rs1057517815
LitVar	rs1057517815
Map	rs1057517815
PheGenI	rs1057517815
Biobank	rs1057517815
1000 genomes	rs1057517815
hgdp	rs1057517815
ensembl	rs1057517815
geneview	rs1057517815
scholar	rs1057517815
google	rs1057517815
pharmgkb	rs1057517815
gwascentral	rs1057517815
openSNP	rs1057517815
23andMe	rs1057517815
SNPshot	rs1057517815
SNPdbe	rs1057517815
MSV3d	rs1057517815
GWAS Ctlg	rs1057517815

Max Magnitude

0

ClinVar
Risk	rs1057517815(G;G)
Alt	rs1057517815(G;G)
Reference	Rs1057517815(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RNASEH2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.51504811A>G
CLNSRC
CLNACC	RCV000414685.1,