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rs554826646

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs554826646(G;T)
Make rs554826646(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position232524355
GeneCHRND, PRSS56
is asnp
is mentioned by
dbSNPrs554826646
ebirs554826646
HLIrs554826646
Exacrs554826646
Varsomers554826646
Maprs554826646
PheGenIrs554826646
hapmaprs554826646
1000 genomesrs554826646
hgdprs554826646
ensemblrs554826646
gopubmedrs554826646
geneviewrs554826646
scholarrs554826646
googlers554826646
pharmgkbrs554826646
gwascentralrs554826646
openSNPrs554826646
23andMers554826646
23andMe allrs554826646
SNP Nexus

SNPshotrs554826646
SNPdbers554826646
MSV3drs554826646
GWAS Ctlgrs554826646
Max Magnitude0
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,