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rs587778805

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587778805(A;A)
Make rs587778805(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position155803625
GeneLOC105375595, SHH
is asnp
is mentioned by
dbSNPrs587778805
ebirs587778805
HLIrs587778805
Exacrs587778805
Varsomers587778805
Maprs587778805
PheGenIrs587778805
hapmaprs587778805
1000 genomesrs587778805
hgdprs587778805
ensemblrs587778805
gopubmedrs587778805
geneviewrs587778805
scholarrs587778805
googlers587778805
pharmgkbrs587778805
gwascentralrs587778805
openSNPrs587778805
23andMers587778805
23andMe allrs587778805
SNP Nexus

SNPshotrs587778805
SNPdbers587778805
MSV3drs587778805
GWAS Ctlgrs587778805
Max Magnitude0
ClinVar
Risk rs587778805(A;A)
Alt rs587778805(A;A)
Reference rs587778805(G;G)
Significance Pathogenic
Disease Holoprosencephaly 3
Variation info
Gene SHH
CLNDBN Holoprosencephaly 3
Reversed 1
HGVS NC_000007.13:g.155596319C>T
CLNSRC
CLNACC RCV000056132.1,