Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520536(C;G)
Make rs1057520536(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position38414186
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1057520536
dbSNP (old)rs1057520536
ClinGenrs1057520536
ebirs1057520536
HLIrs1057520536
Exacrs1057520536
Gnomadrs1057520536
Varsomers1057520536
LitVarrs1057520536
Maprs1057520536
PheGenIrs1057520536
Biobankrs1057520536
1000 genomesrs1057520536
hgdprs1057520536
ensemblrs1057520536
gopubmedrs1057520536
geneviewrs1057520536
scholarrs1057520536
googlers1057520536
pharmgkbrs1057520536
gwascentralrs1057520536
openSNPrs1057520536
23andMers1057520536
23andMe allrs1057520536
SNPshotrs1057520536
SNPdbers1057520536
MSV3drs1057520536
GWAS Ctlgrs1057520536
Max Magnitude0
ClinVar
Risk rs1057520536(G;G)
Alt rs1057520536(G;G)
Reference Rs1057520536(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38271704G>C
CLNSRC
CLNACC RCV000423621.1,