rs121909294

Orientation

plus

Stabilized

plus

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

Make rs121909294(A;A)

Make rs121909294(A;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

15440524

Gene

CTRC

is a	snp
is	mentioned by
dbSNP	rs121909294
dbSNP (classic)	rs121909294
ClinGen	rs121909294
ebi	rs121909294
HLI	rs121909294
Exac	rs121909294
Gnomad	rs121909294
Varsome	rs121909294
LitVar	rs121909294
Map	rs121909294
PheGenI	rs121909294
Biobank	rs121909294
1000 genomes	rs121909294
hgdp	rs121909294
ensembl	rs121909294
geneview	rs121909294
scholar	rs121909294
google	rs121909294
pharmgkb	rs121909294
gwascentral	rs121909294
openSNP	rs121909294
23andMe	rs121909294
SNPshot	rs121909294
SNPdbe	rs121909294
MSV3d	rs121909294
GWAS Ctlg	rs121909294

Max Magnitude

0

OMIM	601405
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121909294(A;A) rs121909294(T;T)
Alt	rs121909294(A;A) rs121909294(T;T)
Reference	Rs121909294(G;G)
Significance	Other
Disease	Pancreatitis Hereditary pancreatitis
Variation	info
Gene	CTRC
CLNDBN	Pancreatitis, chronic, susceptibility to Hereditary pancreatitis
Reversed	0
HGVS	NC_000001.10:g.15767020G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008659.2, RCV000119047.2,