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rs876661333

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661333(A;A)
Make rs876661333(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38414828
GeneFGFR1
is asnp
is mentioned by
dbSNPrs876661333
ebirs876661333
HLIrs876661333
Exacrs876661333
Varsomers876661333
Maprs876661333
PheGenIrs876661333
hapmaprs876661333
1000 genomesrs876661333
hgdprs876661333
ensemblrs876661333
gopubmedrs876661333
geneviewrs876661333
scholarrs876661333
googlers876661333
pharmgkbrs876661333
gwascentralrs876661333
openSNPrs876661333
23andMers876661333
23andMe allrs876661333
SNP Nexus

SNPshotrs876661333
SNPdbers876661333
MSV3drs876661333
GWAS Ctlgrs876661333
Max Magnitude0
ClinVar
Risk rs876661333(A;A)
Alt rs876661333(A;A)
Reference rs876661333(G;G)
Significance Probable-Pathogenic
Disease microform holoprosencephaly
Variation info
Gene FGFR1
CLNDBN microform holoprosencephaly
Reversed 1
HGVS NC_000008.10:g.38272346C>T
CLNSRC
CLNACC RCV000223914.1,