rs515726209

Orientation

plus

Stabilized

plus

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

Make rs515726209(A;A)

Make rs515726209(A;G)

Reference

GRCh38 38.1/142

Chromosome

1

Position

15440577

Gene

CTRC

is a	snp
is	mentioned by
dbSNP	rs515726209
dbSNP (classic)	rs515726209
ClinGen	rs515726209
ebi	rs515726209
HLI	rs515726209
Exac	rs515726209
Gnomad	rs515726209
Varsome	rs515726209
LitVar	rs515726209
Map	rs515726209
PheGenI	rs515726209
Biobank	rs515726209
1000 genomes	rs515726209
hgdp	rs515726209
ensembl	rs515726209
geneview	rs515726209
scholar	rs515726209
google	rs515726209
pharmgkb	rs515726209
gwascentral	rs515726209
openSNP	rs515726209
23andMe	rs515726209
SNPshot	rs515726209
SNPdbe	rs515726209
MSV3d	rs515726209
GWAS Ctlg	rs515726209

Max Magnitude

0

ClinVar
Risk	rs515726209(A;A)
Alt	rs515726209(A;A)
Reference	Rs515726209(G;G)
Significance	Pathogenic
Disease	Hereditary pancreatitis
Variation	info
Gene	CTRC
CLNDBN	Hereditary pancreatitis
Reversed	0
HGVS	NC_000001.10:g.15767073G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000119044.2,