Have questions? Visit https://www.reddit.com/r/SNPedia

rs1060499564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1060499564(-;-)
Make rs1060499564(-;AG)
Make rs1060499564(AG;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position99984967
GeneZIC2
is asnp
is mentioned by
dbSNPrs1060499564
dbSNP (old)rs1060499564
ClinGenrs1060499564
ebirs1060499564
HLIrs1060499564
Exacrs1060499564
Gnomadrs1060499564
Varsomers1060499564
LitVarrs1060499564
Maprs1060499564
PheGenIrs1060499564
Biobankrs1060499564
1000 genomesrs1060499564
hgdprs1060499564
ensemblrs1060499564
gopubmedrs1060499564
geneviewrs1060499564
scholarrs1060499564
googlers1060499564
pharmgkbrs1060499564
gwascentralrs1060499564
openSNPrs1060499564
23andMers1060499564
23andMe allrs1060499564
SNPshotrs1060499564
SNPdbers1060499564
MSV3drs1060499564
GWAS Ctlgrs1060499564
Max Magnitude0
ClinVar
Risk rs1060499564(-;-)
Alt rs1060499564(-;-)
Reference Rs1060499564(GA;GA)
Significance Probable-Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100637221_100637222delAG
CLNSRC
CLNACC RCV000453235.1,