rs1057517810

Orientation

plus

Stabilized

plus

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

Make rs1057517810(A;G)

Make rs1057517810(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

112230677

Gene

PTS

is a	snp
is	mentioned by
dbSNP	rs1057517810
dbSNP (classic)	rs1057517810
ClinGen	rs1057517810
ebi	rs1057517810
HLI	rs1057517810
Exac	rs1057517810
Gnomad	rs1057517810
Varsome	rs1057517810
LitVar	rs1057517810
Map	rs1057517810
PheGenI	rs1057517810
Biobank	rs1057517810
1000 genomes	rs1057517810
hgdp	rs1057517810
ensembl	rs1057517810
geneview	rs1057517810
scholar	rs1057517810
google	rs1057517810
pharmgkb	rs1057517810
gwascentral	rs1057517810
openSNP	rs1057517810
23andMe	rs1057517810
SNPshot	rs1057517810
SNPdbe	rs1057517810
MSV3d	rs1057517810
GWAS Ctlg	rs1057517810

Max Magnitude

0

ClinVar
Risk	rs1057517810(G;G)
Alt	rs1057517810(G;G)
Reference	Rs1057517810(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PTS
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.112101400A>G
CLNSRC
CLNACC	RCV000413378.1,