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rs876661332

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661332(G;T)
Make rs876661332(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38417968
GeneFGFR1
is asnp
is mentioned by
dbSNPrs876661332
ebirs876661332
HLIrs876661332
Exacrs876661332
Varsomers876661332
Maprs876661332
PheGenIrs876661332
hapmaprs876661332
1000 genomesrs876661332
hgdprs876661332
ensemblrs876661332
gopubmedrs876661332
geneviewrs876661332
scholarrs876661332
googlers876661332
pharmgkbrs876661332
gwascentralrs876661332
openSNPrs876661332
23andMers876661332
23andMe allrs876661332
SNP Nexus

SNPshotrs876661332
SNPdbers876661332
MSV3drs876661332
GWAS Ctlgrs876661332
Max Magnitude0
ClinVar
Risk rs876661332(T;T)
Alt rs876661332(T;T)
Reference rs876661332(G;G)
Significance Probable-Pathogenic
Disease Hartsfield syndrome
Variation info
Gene FGFR1
CLNDBN Hartsfield syndrome
Reversed 1
HGVS NC_000008.10:g.38275486C>A
CLNSRC
CLNACC RCV000223739.1,