rs202058123

Orientation

plus

Stabilized

plus

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

Make rs202058123(A;A)

Make rs202058123(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

15445606

Gene

CTRC

is a	snp
is	mentioned by
dbSNP	rs202058123
dbSNP (classic)	rs202058123
ClinGen	rs202058123
ebi	rs202058123
HLI	rs202058123
Exac	rs202058123
Gnomad	rs202058123
Varsome	rs202058123
LitVar	rs202058123
Map	rs202058123
PheGenI	rs202058123
Biobank	rs202058123
1000 genomes	rs202058123
hgdp	rs202058123
ensembl	rs202058123
geneview	rs202058123
scholar	rs202058123
google	rs202058123
pharmgkb	rs202058123
gwascentral	rs202058123
openSNP	rs202058123
23andMe	rs202058123
SNPshot	rs202058123
SNPdbe	rs202058123
MSV3d	rs202058123
GWAS Ctlg	rs202058123

Max Magnitude

0

ClinVar
Risk	rs202058123(A;A) rs202058123(C;C)
Alt	rs202058123(A;A) rs202058123(C;C)
Reference	Rs202058123(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CTRC
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.15772101G>A; NC_000001.10:g.15772101G>C
CLNSRC
CLNACC	RCV000493312.1, RCV000483666.1,