rs1057520687

Orientation

minus

Stabilized

minus

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

Make rs1057520687(C;C)

Make rs1057520687(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

66866191

Gene

PC

is a	snp
is	mentioned by
dbSNP	rs1057520687
dbSNP (classic)	rs1057520687
ClinGen	rs1057520687
ebi	rs1057520687
HLI	rs1057520687
Exac	rs1057520687
Gnomad	rs1057520687
Varsome	rs1057520687
LitVar	rs1057520687
Map	rs1057520687
PheGenI	rs1057520687
Biobank	rs1057520687
1000 genomes	rs1057520687
hgdp	rs1057520687
ensembl	rs1057520687
geneview	rs1057520687
scholar	rs1057520687
google	rs1057520687
pharmgkb	rs1057520687
gwascentral	rs1057520687
openSNP	rs1057520687
23andMe	rs1057520687
SNPshot	rs1057520687
SNPdbe	rs1057520687
MSV3d	rs1057520687
GWAS Ctlg	rs1057520687

Max Magnitude

0

ClinVar
Risk	rs1057520687(C;C)
Alt	rs1057520687(C;C)
Reference	Rs1057520687(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PC
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.66633662A>G
CLNSRC
CLNACC	RCV000433773.1,