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rs876661330

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661330(C;T)
Make rs876661330(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position101771522
GeneFGF8, LOC105378457
is asnp
is mentioned by
dbSNPrs876661330
ebirs876661330
HLIrs876661330
Exacrs876661330
Varsomers876661330
Maprs876661330
PheGenIrs876661330
hapmaprs876661330
1000 genomesrs876661330
hgdprs876661330
ensemblrs876661330
gopubmedrs876661330
geneviewrs876661330
scholarrs876661330
googlers876661330
pharmgkbrs876661330
gwascentralrs876661330
openSNPrs876661330
23andMers876661330
23andMe allrs876661330
SNP Nexus

SNPshotrs876661330
SNPdbers876661330
MSV3drs876661330
GWAS Ctlgrs876661330
Max Magnitude0
ClinVar
Risk rs876661330(T;T)
Alt rs876661330(T;T)
Reference rs876661330(C;C)
Significance Probable-Pathogenic
Disease Holoprosencephaly
Variation info
Gene FGF8
CLNDBN Holoprosencephaly
Reversed 1
HGVS NC_000010.10:g.103531279G>A
CLNSRC
CLNACC RCV000223728.1,