rs515726210

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(ACACCCGCAAGAAGCCGGTAGTCT;ACACCCGCAAGAAGCCGGTAGTCT)	0	common in clinvar
(CAAGAAGCCGGTAGTCTACACCCG;CAAGAAGCCGGTAGTCTACACCCG)	0	common in clinvar

Make rs515726210(-;-)

Make rs515726210(-;CAAGAAGCCGGTAGTCTACACCCG)

Reference

GRCh38 38.1/142

Chromosome

1

Position

15445695

Gene

CTRC

is a	snp
is	mentioned by
dbSNP	rs515726210
dbSNP (classic)	rs515726210
ClinGen	rs515726210
ebi	rs515726210
HLI	rs515726210
Exac	rs515726210
Gnomad	rs515726210
Varsome	rs515726210
LitVar	rs515726210
Map	rs515726210
PheGenI	rs515726210
Biobank	rs515726210
1000 genomes	rs515726210
hgdp	rs515726210
ensembl	rs515726210
geneview	rs515726210
scholar	rs515726210
google	rs515726210
pharmgkb	rs515726210
gwascentral	rs515726210
openSNP	rs515726210
23andMe	rs515726210
SNPshot	rs515726210
SNPdbe	rs515726210
MSV3d	rs515726210
GWAS Ctlg	rs515726210

Max Magnitude

0

ClinVar
Risk	rs515726210(-;-) Rs515726210(ACACCCGCAAGAAGCCGGTAGTCT;ACACCCGCAAGAAGCCGGTAGTCT)
Alt	rs515726210(-;-) Rs515726210(ACACCCGCAAGAAGCCGGTAGTCT;ACACCCGCAAGAAGCCGGTAGTCT)
Reference	Rs515726210(CAAGAAGCCGGTAGTCTACACCCG;CAAGAAGCCGGTAGTCTACACCCG)
Significance	Pathogenic
Disease	Hereditary pancreatitis
Variation	info
Gene	CTRC
CLNDBN	Hereditary pancreatitis
Reversed	0
HGVS	NC_000001.10:g.15772190_15772213del24
CLNSRC	ClinVar
CLNACC	RCV000119046.2,