Have questions? Visit https://www.reddit.com/r/SNPedia

rs876661328

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661328(A;A)
Make rs876661328(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position101774752
GeneFGF8
is asnp
is mentioned by
dbSNPrs876661328
ebirs876661328
HLIrs876661328
Exacrs876661328
Varsomers876661328
Maprs876661328
PheGenIrs876661328
hapmaprs876661328
1000 genomesrs876661328
hgdprs876661328
ensemblrs876661328
gopubmedrs876661328
geneviewrs876661328
scholarrs876661328
googlers876661328
pharmgkbrs876661328
gwascentralrs876661328
openSNPrs876661328
23andMers876661328
23andMe allrs876661328
SNP Nexus

SNPshotrs876661328
SNPdbers876661328
MSV3drs876661328
GWAS Ctlgrs876661328
Max Magnitude0
ClinVar
Risk rs876661328(A;A)
Alt rs876661328(A;A)
Reference rs876661328(C;C)
Significance Probable-Pathogenic
Disease Semilobar holoprosencephaly
Variation info
Gene FGF8
CLNDBN Semilobar holoprosencephaly
Reversed 1
HGVS NC_000010.10:g.103534509G>T
CLNSRC
CLNACC RCV000223804.1,