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rs587778803

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587778803(C;T)
Make rs587778803(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position155803664
GeneLOC105375595, SHH
is asnp
is mentioned by
dbSNPrs587778803
ebirs587778803
HLIrs587778803
Exacrs587778803
Varsomers587778803
Maprs587778803
PheGenIrs587778803
hapmaprs587778803
1000 genomesrs587778803
hgdprs587778803
ensemblrs587778803
gopubmedrs587778803
geneviewrs587778803
scholarrs587778803
googlers587778803
pharmgkbrs587778803
gwascentralrs587778803
openSNPrs587778803
23andMers587778803
23andMe allrs587778803
SNP Nexus

SNPshotrs587778803
SNPdbers587778803
MSV3drs587778803
GWAS Ctlgrs587778803
Max Magnitude0
ClinVar
Risk rs587778803(T;T)
Alt rs587778803(T;T)
Reference rs587778803(C;C)
Significance Pathogenic
Disease Holoprosencephaly 3
Variation info
Gene SHH
CLNDBN Holoprosencephaly 3
Reversed 1
HGVS NC_000007.13:g.155596358G>A
CLNSRC
CLNACC RCV000056128.1,