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rs876661334

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661334(A;A)
Make rs876661334(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38414778
GeneFGFR1
is asnp
is mentioned by
dbSNPrs876661334
ebirs876661334
HLIrs876661334
Exacrs876661334
Varsomers876661334
Maprs876661334
PheGenIrs876661334
hapmaprs876661334
1000 genomesrs876661334
hgdprs876661334
ensemblrs876661334
gopubmedrs876661334
geneviewrs876661334
scholarrs876661334
googlers876661334
pharmgkbrs876661334
gwascentralrs876661334
openSNPrs876661334
23andMers876661334
23andMe allrs876661334
SNP Nexus

SNPshotrs876661334
SNPdbers876661334
MSV3drs876661334
GWAS Ctlgrs876661334
Max Magnitude0
ClinVar
Risk rs876661334(A;A)
Alt rs876661334(A;A)
Reference rs876661334(G;G)
Significance Probable-Pathogenic
Disease Semilobar holoprosencephaly
Variation info
Gene FGFR1
CLNDBN Semilobar holoprosencephaly
Reversed 1
HGVS NC_000008.10:g.38272296C>T
CLNSRC
CLNACC RCV000223775.1,