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rs869025669

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025669(C;C)
Make rs869025669(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38427970
GeneFGFR1
is asnp
is mentioned by
dbSNPrs869025669
ebirs869025669
HLIrs869025669
Exacrs869025669
Varsomers869025669
Maprs869025669
PheGenIrs869025669
hapmaprs869025669
1000 genomesrs869025669
hgdprs869025669
ensemblrs869025669
gopubmedrs869025669
geneviewrs869025669
scholarrs869025669
googlers869025669
pharmgkbrs869025669
gwascentralrs869025669
openSNPrs869025669
23andMers869025669
23andMe allrs869025669
SNP Nexus

SNPshotrs869025669
SNPdbers869025669
MSV3drs869025669
GWAS Ctlgrs869025669
Max Magnitude0
ClinVar
Risk rs869025669(C;C)
Alt rs869025669(C;C)
Reference rs869025669(T;T)
Significance Pathogenic
Disease Hartsfield syndrome
Variation info
Gene FGFR1
CLNDBN Hartsfield syndrome
Reversed 1
HGVS NC_000008.10:g.38285488A>G
CLNSRC
CLNACC RCV000208879.1,