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rs876661331

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661331(A;A)
Make rs876661331(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position101770447
GeneFGF8, LOC105378457
is asnp
is mentioned by
dbSNPrs876661331
ebirs876661331
HLIrs876661331
Exacrs876661331
Varsomers876661331
Maprs876661331
PheGenIrs876661331
hapmaprs876661331
1000 genomesrs876661331
hgdprs876661331
ensemblrs876661331
gopubmedrs876661331
geneviewrs876661331
scholarrs876661331
googlers876661331
pharmgkbrs876661331
gwascentralrs876661331
openSNPrs876661331
23andMers876661331
23andMe allrs876661331
SNP Nexus

SNPshotrs876661331
SNPdbers876661331
MSV3drs876661331
GWAS Ctlgrs876661331
Max Magnitude0
ClinVar
Risk rs876661331(A;A)
Alt rs876661331(A;A)
Reference rs876661331(G;G)
Significance Probable-Pathogenic
Disease Holoprosencephaly
Variation info
Gene FGF8
CLNDBN Holoprosencephaly
Reversed 1
HGVS NC_000010.10:g.103530204C>T
CLNSRC
CLNACC RCV000223812.1,