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rs587778799

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778799(C;C)
Make rs587778799(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position155806296
GeneSHH
is asnp
is mentioned by
dbSNPrs587778799
ebirs587778799
HLIrs587778799
Exacrs587778799
Varsomers587778799
Maprs587778799
PheGenIrs587778799
hapmaprs587778799
1000 genomesrs587778799
hgdprs587778799
ensemblrs587778799
gopubmedrs587778799
geneviewrs587778799
scholarrs587778799
googlers587778799
pharmgkbrs587778799
gwascentralrs587778799
openSNPrs587778799
23andMers587778799
23andMe allrs587778799
SNP Nexus

SNPshotrs587778799
SNPdbers587778799
MSV3drs587778799
GWAS Ctlgrs587778799
Max Magnitude0
ClinVar
Risk rs587778799(C;C)
Alt rs587778799(C;C)
Reference rs587778799(G;G)
Significance Pathogenic
Disease Holoprosencephaly 3
Variation info
Gene SHH
CLNDBN Holoprosencephaly 3
Reversed 1
HGVS NC_000007.13:g.155598990C>G
CLNSRC
CLNACC RCV000056121.1,