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rs1085307522

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position22190507
GenePHEX
is asnp
is mentioned by
dbSNPrs1085307522
dbSNP (old)rs1085307522
ClinGenrs1085307522
ebirs1085307522
HLIrs1085307522
Exacrs1085307522
Gnomadrs1085307522
Varsomers1085307522
Maprs1085307522
PheGenIrs1085307522
Biobankrs1085307522
1000 genomesrs1085307522
hgdprs1085307522
ensemblrs1085307522
gopubmedrs1085307522
geneviewrs1085307522
scholarrs1085307522
googlers1085307522
pharmgkbrs1085307522
gwascentralrs1085307522
openSNPrs1085307522
23andMers1085307522
23andMe allrs1085307522
SNPshotrs1085307522
SNPdbers1085307522
MSV3drs1085307522
GWAS Ctlgrs1085307522
Max Magnitude0
ClinVar
Risk rs1085307522(C;C)
Alt rs1085307522(C;C)
Reference Rs1085307522(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22208624G>C
CLNSRC
CLNACC RCV000489771.1,