rs397507442

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	4.4	Hereditary pancreatitis

Make rs397507442(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

142750579

Gene

PRSS1

is a	snp
is	mentioned by
dbSNP	rs397507442
dbSNP (classic)	rs397507442
ClinGen	rs397507442
ebi	rs397507442
HLI	rs397507442
Exac	rs397507442
Gnomad	rs397507442
Varsome	rs397507442
LitVar	rs397507442
Map	rs397507442
PheGenI	rs397507442
Biobank	rs397507442
1000 genomes	rs397507442
hgdp	rs397507442
ensembl	rs397507442
geneview	rs397507442
scholar	rs397507442
google	rs397507442
pharmgkb	rs397507442
gwascentral	rs397507442
openSNP	rs397507442
23andMe	rs397507442
SNPshot	rs397507442
SNPdbe	rs397507442
MSV3d	rs397507442
GWAS Ctlg	rs397507442

Max Magnitude

4.4

c.65A>G, p.Asp22Gly and D22G

ClinVar
Risk	rs397507442(G;G)
Alt	rs397507442(G;G)
Reference	Rs397507442(A;A)
Significance	Pathogenic
Disease	Hereditary pancreatitis
Variation	info
Gene	PRSS1
CLNDBN	Hereditary pancreatitis
Reversed	0
HGVS	NC_000007.13:g.142458430A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000031922.1,