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rs876661335

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661335(A;A)
Make rs876661335(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38414264
GeneFGFR1
is asnp
is mentioned by
dbSNPrs876661335
ebirs876661335
HLIrs876661335
Exacrs876661335
Varsomers876661335
Maprs876661335
PheGenIrs876661335
hapmaprs876661335
1000 genomesrs876661335
hgdprs876661335
ensemblrs876661335
gopubmedrs876661335
geneviewrs876661335
scholarrs876661335
googlers876661335
pharmgkbrs876661335
gwascentralrs876661335
openSNPrs876661335
23andMers876661335
23andMe allrs876661335
SNP Nexus

SNPshotrs876661335
SNPdbers876661335
MSV3drs876661335
GWAS Ctlgrs876661335
Max Magnitude0
ClinVar
Risk rs876661335(A;A)
Alt rs876661335(A;A)
Reference rs876661335(G;G)
Significance Probable-Pathogenic
Disease Holoprosencephaly
Variation info
Gene FGFR1
CLNDBN Holoprosencephaly
Reversed 1
HGVS NC_000008.10:g.38271782C>T
CLNSRC
CLNACC RCV000223865.1,