rs554826646

Orientation

plus

Stabilized

plus

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

Make rs554826646(G;T)

Make rs554826646(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

232524355

Gene	CHRND, PRSS56

is a	snp
is	mentioned by
dbSNP	rs554826646
dbSNP (classic)	rs554826646
ClinGen	rs554826646
ebi	rs554826646
HLI	rs554826646
Exac	rs554826646
Gnomad	rs554826646
Varsome	rs554826646
LitVar	rs554826646
Map	rs554826646
PheGenI	rs554826646
Biobank	rs554826646
1000 genomes	rs554826646
hgdp	rs554826646
ensembl	rs554826646
geneview	rs554826646
scholar	rs554826646
google	rs554826646
pharmgkb	rs554826646
gwascentral	rs554826646
openSNP	rs554826646
23andMe	rs554826646
SNPshot	rs554826646
SNPdbe	rs554826646
MSV3d	rs554826646
GWAS Ctlg	rs554826646

Max Magnitude

0

ClinVar
Risk	rs554826646(T;T)
Alt	rs554826646(T;T)
Reference	Rs554826646(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHRND PRSS56
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.233389065G>T
CLNSRC
CLNACC	RCV000171337.1,