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rs587778789

From SNPedia

Orientationminus
Geno Mag Summary
(TCTCCTCG;TCTCCTCG) 0 common in clinvar
Make rs587778789(-;-)
Make rs587778789(-;TCTCCTCG)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position155812078
GeneSHH
is asnp
is mentioned by
dbSNPrs587778789
ebirs587778789
HLIrs587778789
Exacrs587778789
Varsomers587778789
Maprs587778789
PheGenIrs587778789
hapmaprs587778789
1000 genomesrs587778789
hgdprs587778789
ensemblrs587778789
gopubmedrs587778789
geneviewrs587778789
scholarrs587778789
googlers587778789
pharmgkbrs587778789
gwascentralrs587778789
openSNPrs587778789
23andMers587778789
23andMe allrs587778789
SNP Nexus

SNPshotrs587778789
SNPdbers587778789
MSV3drs587778789
GWAS Ctlgrs587778789
Max Magnitude0
ClinVar
Risk rs587778789(;)
Alt rs587778789(;)
Reference rs587778789(TCTCCTCG;TCTCCTCG)
Significance Pathogenic
Disease Holoprosencephaly 3
Variation info
Gene SHH
CLNDBN Holoprosencephaly 3
Reversed 1
HGVS NC_000007.13:g.155604772_155604779delCGAGGAGA
CLNSRC
CLNACC RCV000056099.1,