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rs397515481

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515481(C;C)
Make rs397515481(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position38428048
GeneFGFR1
is asnp
is mentioned by
dbSNPrs397515481
ebirs397515481
HLIrs397515481
Exacrs397515481
Varsomers397515481
Maprs397515481
PheGenIrs397515481
hapmaprs397515481
1000 genomesrs397515481
hgdprs397515481
ensemblrs397515481
gopubmedrs397515481
geneviewrs397515481
scholarrs397515481
googlers397515481
pharmgkbrs397515481
gwascentralrs397515481
openSNPrs397515481
23andMers397515481
23andMe allrs397515481
SNP Nexus

SNPshotrs397515481
SNPdbers397515481
MSV3drs397515481
GWAS Ctlgrs397515481
Max Magnitude0
ClinVar
Risk rs397515481(C;C)
Alt rs397515481(C;C)
Reference rs397515481(T;T)
Significance Pathogenic
Disease Hartsfield syndrome
Variation info
Gene FGFR1
CLNDBN Hartsfield syndrome
Reversed 1
HGVS NC_000008.10:g.38285566A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000056314.28,