rs121909293

Orientation

plus

Stabilized

plus

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

Make rs121909293(C;T)

Make rs121909293(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

15445717

Gene

CTRC

is a	snp
is	mentioned by
dbSNP	rs121909293
dbSNP (classic)	rs121909293
ClinGen	rs121909293
ebi	rs121909293
HLI	rs121909293
Exac	rs121909293
Gnomad	rs121909293
Varsome	rs121909293
LitVar	rs121909293
Map	rs121909293
PheGenI	rs121909293
Biobank	rs121909293
1000 genomes	rs121909293
hgdp	rs121909293
ensembl	rs121909293
geneview	rs121909293
scholar	rs121909293
google	rs121909293
pharmgkb	rs121909293
gwascentral	rs121909293
openSNP	rs121909293
23andMe	rs121909293
SNPshot	rs121909293
SNPdbe	rs121909293
MSV3d	rs121909293
GWAS Ctlg	rs121909293

GMAF

0.004132

Max Magnitude

0

OMIM	601405
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909293(T;T)
Alt	rs121909293(T;T)
Reference	Rs121909293(C;C)
Significance	Other
Disease	Pancreatitis Hereditary pancreatitis
Variation	info
Gene	CTRC
CLNDBN	Pancreatitis, chronic, susceptibility to Hereditary pancreatitis
Reversed	0
HGVS	NC_000001.10:g.15772212C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008657.2, RCV000119045.3,