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rs876661329

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661329(C;T)
Make rs876661329(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position101771551
GeneFGF8, LOC105378457
is asnp
is mentioned by
dbSNPrs876661329
ebirs876661329
HLIrs876661329
Exacrs876661329
Varsomers876661329
Maprs876661329
PheGenIrs876661329
hapmaprs876661329
1000 genomesrs876661329
hgdprs876661329
ensemblrs876661329
gopubmedrs876661329
geneviewrs876661329
scholarrs876661329
googlers876661329
pharmgkbrs876661329
gwascentralrs876661329
openSNPrs876661329
23andMers876661329
23andMe allrs876661329
SNP Nexus

SNPshotrs876661329
SNPdbers876661329
MSV3drs876661329
GWAS Ctlgrs876661329
Max Magnitude0
ClinVar
Risk rs876661329(T;T)
Alt rs876661329(T;T)
Reference rs876661329(C;C)
Significance Probable-Pathogenic
Disease Semilobar holoprosencephaly
Variation info
Gene FGF8
CLNDBN Semilobar holoprosencephaly
Reversed 1
HGVS NC_000010.10:g.103531308G>A
CLNSRC
CLNACC RCV000223893.1,