rs606231345

Merged into

rs199769221

Orientation

plus

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

Make rs606231345(A;A)

Make rs606231345(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

142751920

Gene

PRSS1

is a	snp
is	mentioned by
dbSNP	rs606231345
dbSNP (classic)	rs606231345
ClinGen	rs606231345
ebi	rs606231345
HLI	rs606231345
Exac	rs606231345
Gnomad	rs606231345
Varsome	rs606231345
LitVar	rs606231345
Map	rs606231345
PheGenI	rs606231345
Biobank	rs606231345
1000 genomes	rs606231345
hgdp	rs606231345
ensembl	rs606231345
geneview	rs606231345
scholar	rs606231345
google	rs606231345
pharmgkb	rs606231345
gwascentral	rs606231345
openSNP	rs606231345
23andMe	rs606231345
SNPshot	rs606231345
SNPdbe	rs606231345
MSV3d	rs606231345
GWAS Ctlg	rs606231345

Status

Merged into rs199769221

Max Magnitude

0

ClinVar
Risk	rs606231345(C;C)
Alt	rs606231345(C;C)
Reference	Rs606231345(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary pancreatitis
Variation	info
Gene	PRSS1
CLNDBN	Hereditary pancreatitis
Reversed	0
HGVS	NC_000007.14:g.142751920G>C
CLNSRC	ClinVar
CLNACC	RCV000149411.1,