rs577173144

Orientation

plus

Stabilized

plus

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

Make rs577173144(A;A)

Make rs577173144(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

95799275

Gene

CEP57

is a	snp
is	mentioned by
dbSNP	rs577173144
dbSNP (classic)	rs577173144
ClinGen	rs577173144
ebi	rs577173144
HLI	rs577173144
Exac	rs577173144
Gnomad	rs577173144
Varsome	rs577173144
LitVar	rs577173144
Map	rs577173144
PheGenI	rs577173144
Biobank	rs577173144
1000 genomes	rs577173144
hgdp	rs577173144
ensembl	rs577173144
geneview	rs577173144
scholar	rs577173144
google	rs577173144
pharmgkb	rs577173144
gwascentral	rs577173144
openSNP	rs577173144
23andMe	rs577173144
SNPshot	rs577173144
SNPdbe	rs577173144
MSV3d	rs577173144
GWAS Ctlg	rs577173144

Max Magnitude

0

ClinVar
Risk	rs577173144(A;A) rs577173144(C;C)
Alt	rs577173144(A;A) rs577173144(C;C)
Reference	Rs577173144(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CEP57
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.95532439G>C
CLNSRC
CLNACC	RCV000171200.1,