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rs1057521074

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521074(A;A)
Make rs1057521074(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154902063
GeneF8
is asnp
is mentioned by
dbSNPrs1057521074
dbSNP (old)rs1057521074
ClinGenrs1057521074
ebirs1057521074
HLIrs1057521074
Exacrs1057521074
Gnomadrs1057521074
Varsomers1057521074
Maprs1057521074
PheGenIrs1057521074
Biobankrs1057521074
1000 genomesrs1057521074
hgdprs1057521074
ensemblrs1057521074
gopubmedrs1057521074
geneviewrs1057521074
scholarrs1057521074
googlers1057521074
pharmgkbrs1057521074
gwascentralrs1057521074
openSNPrs1057521074
23andMers1057521074
23andMe allrs1057521074
SNPshotrs1057521074
SNPdbers1057521074
MSV3drs1057521074
GWAS Ctlgrs1057521074
Max Magnitude0
ClinVar
Risk rs1057521074(A;A)
Alt rs1057521074(A;A)
Reference Rs1057521074(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene F8
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.154130338C>T
CLNSRC
CLNACC RCV000442362.1,