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rs1064793122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position38421868
GeneFGFR1
is asnp
is mentioned by
dbSNPrs1064793122
dbSNP (old)rs1064793122
ClinGenrs1064793122
ebirs1064793122
HLIrs1064793122
Exacrs1064793122
Gnomadrs1064793122
Varsomers1064793122
Maprs1064793122
PheGenIrs1064793122
Biobankrs1064793122
1000 genomesrs1064793122
hgdprs1064793122
ensemblrs1064793122
gopubmedrs1064793122
geneviewrs1064793122
scholarrs1064793122
googlers1064793122
pharmgkbrs1064793122
gwascentralrs1064793122
openSNPrs1064793122
23andMers1064793122
23andMe allrs1064793122
SNPshotrs1064793122
SNPdbers1064793122
MSV3drs1064793122
GWAS Ctlgrs1064793122
Max Magnitude0
ClinVar
Risk rs1064793122(A;A)
Alt rs1064793122(A;A)
Reference Rs1064793122(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FGFR1
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.38279386C>T
CLNSRC
CLNACC RCV000478577.1,