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rs587778788

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778788(-;-)
Make rs587778788(-;GCTG)
Make rs587778788(GCTG;GCTG)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position155812113
GeneSHH
is asnp
is mentioned by
dbSNPrs587778788
ebirs587778788
HLIrs587778788
Exacrs587778788
Varsomers587778788
Maprs587778788
PheGenIrs587778788
hapmaprs587778788
1000 genomesrs587778788
hgdprs587778788
ensemblrs587778788
gopubmedrs587778788
geneviewrs587778788
scholarrs587778788
googlers587778788
pharmgkbrs587778788
gwascentralrs587778788
openSNPrs587778788
23andMers587778788
23andMe allrs587778788
SNP Nexus

SNPshotrs587778788
SNPdbers587778788
MSV3drs587778788
GWAS Ctlgrs587778788
Max Magnitude0
ClinVar
Risk rs587778788(GCTG;GCTG)
Alt rs587778788(GCTG;GCTG)
Reference rs587778788(;)
Significance Pathogenic
Disease Holoprosencephaly 3
Variation info
Gene SHH
CLNDBN Holoprosencephaly 3
Reversed 1
HGVS NC_000007.13:g.155604807_155604808insCAGC
CLNSRC
CLNACC RCV000056094.1,