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rs1085307642

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position22047174
GenePHEX
is asnp
is mentioned by
dbSNPrs1085307642
dbSNP (old)rs1085307642
ClinGenrs1085307642
ebirs1085307642
HLIrs1085307642
Exacrs1085307642
Gnomadrs1085307642
Varsomers1085307642
Maprs1085307642
PheGenIrs1085307642
Biobankrs1085307642
1000 genomesrs1085307642
hgdprs1085307642
ensemblrs1085307642
gopubmedrs1085307642
geneviewrs1085307642
scholarrs1085307642
googlers1085307642
pharmgkbrs1085307642
gwascentralrs1085307642
openSNPrs1085307642
23andMers1085307642
23andMe allrs1085307642
SNPshotrs1085307642
SNPdbers1085307642
MSV3drs1085307642
GWAS Ctlgrs1085307642
Max Magnitude0
ClinVar
Risk rs1085307642(G;G)
Alt rs1085307642(G;G)
Reference Rs1085307642(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene PHEX
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.22065292T>G
CLNSRC
CLNACC RCV000490200.1,