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rs1057516043

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516043(-;T)
Make rs1057516043(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position110719855
GeneCHRDL1
is asnp
is mentioned by
dbSNPrs1057516043
dbSNP (old)rs1057516043
ClinGenrs1057516043
ebirs1057516043
HLIrs1057516043
Exacrs1057516043
Gnomadrs1057516043
Varsomers1057516043
LitVarrs1057516043
Maprs1057516043
PheGenIrs1057516043
Biobankrs1057516043
1000 genomesrs1057516043
hgdprs1057516043
ensemblrs1057516043
gopubmedrs1057516043
geneviewrs1057516043
scholarrs1057516043
googlers1057516043
pharmgkbrs1057516043
gwascentralrs1057516043
openSNPrs1057516043
23andMers1057516043
23andMe allrs1057516043
SNPshotrs1057516043
SNPdbers1057516043
MSV3drs1057516043
GWAS Ctlgrs1057516043
Max Magnitude0
ClinVar
Risk rs1057516043(T;T)
Alt rs1057516043(T;T)
Reference Rs1057516043(-;-)
Significance Pathogenic
Disease Megalocornea
Variation info
Gene CHRDL1
CLNDBN Megalocornea
Reversed 1
HGVS NC_000023.10:g.109963084dupA
CLNSRC
CLNACC RCV000408611.1,