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rs869025672

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025672(G;G)
Make rs869025672(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38414872
GeneFGFR1
is asnp
is mentioned by
dbSNPrs869025672
ebirs869025672
HLIrs869025672
Exacrs869025672
Varsomers869025672
Maprs869025672
PheGenIrs869025672
hapmaprs869025672
1000 genomesrs869025672
hgdprs869025672
ensemblrs869025672
gopubmedrs869025672
geneviewrs869025672
scholarrs869025672
googlers869025672
pharmgkbrs869025672
gwascentralrs869025672
openSNPrs869025672
23andMers869025672
23andMe allrs869025672
SNP Nexus

SNPshotrs869025672
SNPdbers869025672
MSV3drs869025672
GWAS Ctlgrs869025672
Max Magnitude0
ClinVar
Risk rs869025672(G;G)
Alt rs869025672(G;G)
Reference rs869025672(T;T)
Significance Pathogenic
Disease Hartsfield syndrome
Variation info
Gene FGFR1
CLNDBN Hartsfield syndrome
Reversed 1
HGVS NC_000008.10:g.38272390A>C
CLNSRC
CLNACC RCV000208876.1,