rs774897991

Orientation

plus

Stabilized

plus

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

Make rs774897991(C;T)

Make rs774897991(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

66850413

Gene

PC

is a	snp
is	mentioned by
dbSNP	rs774897991
dbSNP (classic)	rs774897991
ClinGen	rs774897991
ebi	rs774897991
HLI	rs774897991
Exac	rs774897991
Gnomad	rs774897991
Varsome	rs774897991
LitVar	rs774897991
Map	rs774897991
PheGenI	rs774897991
Biobank	rs774897991
1000 genomes	rs774897991
hgdp	rs774897991
ensembl	rs774897991
geneview	rs774897991
scholar	rs774897991
google	rs774897991
pharmgkb	rs774897991
gwascentral	rs774897991
openSNP	rs774897991
23andMe	rs774897991
SNPshot	rs774897991
SNPdbe	rs774897991
MSV3d	rs774897991
GWAS Ctlg	rs774897991

Max Magnitude

0

ClinVar
Risk	rs774897991(T;T)
Alt	rs774897991(T;T)
Reference	Rs774897991(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PC
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.66617884C>T
CLNSRC
CLNACC	RCV000186120.1,