rs267606982

Orientation

plus

Stabilized

plus

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

Make rs267606982(AT;AT)

Make rs267606982(AT;GC)

Reference

GRCh38 38.1/141

Chromosome

7

Position

142751938

Gene

PRSS1

is a	snp
is	mentioned by
dbSNP	rs267606982
dbSNP (classic)	rs267606982
ClinGen	rs267606982
ebi	rs267606982
HLI	rs267606982
Exac	rs267606982
Gnomad	rs267606982
Varsome	rs267606982
LitVar	rs267606982
Map	rs267606982
PheGenI	rs267606982
Biobank	rs267606982
1000 genomes	rs267606982
hgdp	rs267606982
ensembl	rs267606982
geneview	rs267606982
scholar	rs267606982
google	rs267606982
pharmgkb	rs267606982
gwascentral	rs267606982
openSNP	rs267606982
23andMe	rs267606982
SNPshot	rs267606982
SNPdbe	rs267606982
MSV3d	rs267606982
GWAS Ctlg	rs267606982

Max Magnitude

0

ClinVar
Risk	rs267606982(AT;AT)
Alt	rs267606982(AT;AT)
Reference	Rs267606982(GC;GC)
Significance	Pathogenic
Disease	Hereditary pancreatitis
Variation	info
Gene	PRSS1
CLNDBN	Hereditary pancreatitis
Reversed	0
HGVS	NC_000007.13:g.142459789_142459790delGCinsAT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012657.25,