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rs1060499563

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499563(C;T)
Make rs1060499563(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position99982857
GeneZIC2
is asnp
is mentioned by
dbSNPrs1060499563
dbSNP (old)rs1060499563
ClinGenrs1060499563
ebirs1060499563
HLIrs1060499563
Exacrs1060499563
Gnomadrs1060499563
Varsomers1060499563
LitVarrs1060499563
Maprs1060499563
PheGenIrs1060499563
Biobankrs1060499563
1000 genomesrs1060499563
hgdprs1060499563
ensemblrs1060499563
gopubmedrs1060499563
geneviewrs1060499563
scholarrs1060499563
googlers1060499563
pharmgkbrs1060499563
gwascentralrs1060499563
openSNPrs1060499563
23andMers1060499563
23andMe allrs1060499563
SNPshotrs1060499563
SNPdbers1060499563
MSV3drs1060499563
GWAS Ctlgrs1060499563
Max Magnitude0
ClinVar
Risk rs1060499563(T;T)
Alt rs1060499563(T;T)
Reference Rs1060499563(C;C)
Significance Pathogenic
Disease Holoprosencephaly 5
Variation info
Gene ZIC2
CLNDBN Holoprosencephaly 5
Reversed 0
HGVS NC_000013.10:g.100635111C>T
CLNSRC
CLNACC RCV000451172.1,