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rs869025671

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025671(C;C)
Make rs869025671(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position38414876
GeneFGFR1
is asnp
is mentioned by
dbSNPrs869025671
ebirs869025671
HLIrs869025671
Exacrs869025671
Varsomers869025671
Maprs869025671
PheGenIrs869025671
hapmaprs869025671
1000 genomesrs869025671
hgdprs869025671
ensemblrs869025671
gopubmedrs869025671
geneviewrs869025671
scholarrs869025671
googlers869025671
pharmgkbrs869025671
gwascentralrs869025671
openSNPrs869025671
23andMers869025671
23andMe allrs869025671
SNP Nexus

SNPshotrs869025671
SNPdbers869025671
MSV3drs869025671
GWAS Ctlgrs869025671
Max Magnitude0
ClinVar
Risk rs869025671(C;C)
Alt rs869025671(C;C)
Reference rs869025671(G;G)
Significance Pathogenic
Disease Hartsfield syndrome
Variation info
Gene FGFR1
CLNDBN Hartsfield syndrome
Reversed 1
HGVS NC_000008.10:g.38272394C>G
CLNSRC
CLNACC RCV000208873.1,