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rs773009397

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773009397(A;A)
Make rs773009397(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position40397178
GenePRX
is asnp
is mentioned by
dbSNPrs773009397
ebirs773009397
HLIrs773009397
Exacrs773009397
Varsomers773009397
Maprs773009397
PheGenIrs773009397
hapmaprs773009397
1000 genomesrs773009397
hgdprs773009397
ensemblrs773009397
gopubmedrs773009397
geneviewrs773009397
scholarrs773009397
googlers773009397
pharmgkbrs773009397
gwascentralrs773009397
openSNPrs773009397
23andMers773009397
23andMe allrs773009397
SNP Nexus

SNPshotrs773009397
SNPdbers773009397
MSV3drs773009397
GWAS Ctlgrs773009397
Max Magnitude0
ClinVar
Risk rs773009397(A;A)
Alt rs773009397(A;A)
Reference rs773009397(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PRX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.40903085G>A
CLNSRC
CLNACC RCV000235669.1,