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rs1085307637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position44309665
GeneALX4
is asnp
is mentioned by
dbSNPrs1085307637
dbSNP (old)rs1085307637
ClinGenrs1085307637
ebirs1085307637
HLIrs1085307637
Exacrs1085307637
Gnomadrs1085307637
Varsomers1085307637
Maprs1085307637
PheGenIrs1085307637
Biobankrs1085307637
1000 genomesrs1085307637
hgdprs1085307637
ensemblrs1085307637
gopubmedrs1085307637
geneviewrs1085307637
scholarrs1085307637
googlers1085307637
pharmgkbrs1085307637
gwascentralrs1085307637
openSNPrs1085307637
23andMers1085307637
23andMe allrs1085307637
SNPshotrs1085307637
SNPdbers1085307637
MSV3drs1085307637
GWAS Ctlgrs1085307637
Max Magnitude0
ClinVar
Risk rs1085307637(-;-)
Alt rs1085307637(-;-)
Reference Rs1085307637(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ALX4
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.44331215delG
CLNSRC
CLNACC RCV000489069.1,