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rs1060499562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs1060499562(-;-)
Make rs1060499562(-;TG)
Make rs1060499562(TG;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position99984965
GeneZIC2
is asnp
is mentioned by
dbSNPrs1060499562
dbSNP (old)rs1060499562
ClinGenrs1060499562
ebirs1060499562
HLIrs1060499562
Exacrs1060499562
Gnomadrs1060499562
Varsomers1060499562
LitVarrs1060499562
Maprs1060499562
PheGenIrs1060499562
Biobankrs1060499562
1000 genomesrs1060499562
hgdprs1060499562
ensemblrs1060499562
gopubmedrs1060499562
geneviewrs1060499562
scholarrs1060499562
googlers1060499562
pharmgkbrs1060499562
gwascentralrs1060499562
openSNPrs1060499562
23andMers1060499562
23andMe allrs1060499562
SNPshotrs1060499562
SNPdbers1060499562
MSV3drs1060499562
GWAS Ctlgrs1060499562
Max Magnitude0
ClinVar
Risk rs1060499562(-;-)
Alt rs1060499562(-;-)
Reference Rs1060499562(GT;GT)
Significance Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100637219_100637220delTG
CLNSRC
CLNACC RCV000452804.1,