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rs1060499782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs1060499782(-;-)
Make rs1060499782(-;GA)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position232535132
GeneCHRND
is asnp
is mentioned by
dbSNPrs1060499782
dbSNP (old)rs1060499782
ClinGenrs1060499782
ebirs1060499782
HLIrs1060499782
Exacrs1060499782
Gnomadrs1060499782
Varsomers1060499782
LitVarrs1060499782
Maprs1060499782
PheGenIrs1060499782
Biobankrs1060499782
1000 genomesrs1060499782
hgdprs1060499782
ensemblrs1060499782
gopubmedrs1060499782
geneviewrs1060499782
scholarrs1060499782
googlers1060499782
pharmgkbrs1060499782
gwascentralrs1060499782
openSNPrs1060499782
23andMers1060499782
23andMe allrs1060499782
SNPshotrs1060499782
SNPdbers1060499782
MSV3drs1060499782
GWAS Ctlgrs1060499782
Max Magnitude0
ClinVar
Risk rs1060499782(-;-)
Alt rs1060499782(-;-)
Reference Rs1060499782(GA;GA)
Significance Probable-Pathogenic
Disease Lethal multiple pterygium syndrome
Variation info
Gene CHRND
CLNDBN Lethal multiple pterygium syndrome
Reversed 0
HGVS NC_000002.11:g.233399842_233399843delGA
CLNSRC
CLNACC RCV000454340.1,