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rs1057524378

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524378(C;C)
Make rs1057524378(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154350907
GeneFLNA
is asnp
is mentioned by
dbSNPrs1057524378
dbSNP (old)rs1057524378
ClinGenrs1057524378
ebirs1057524378
HLIrs1057524378
Exacrs1057524378
Gnomadrs1057524378
Varsomers1057524378
Maprs1057524378
PheGenIrs1057524378
Biobankrs1057524378
1000 genomesrs1057524378
hgdprs1057524378
ensemblrs1057524378
gopubmedrs1057524378
geneviewrs1057524378
scholarrs1057524378
googlers1057524378
pharmgkbrs1057524378
gwascentralrs1057524378
openSNPrs1057524378
23andMers1057524378
23andMe allrs1057524378
SNPshotrs1057524378
SNPdbers1057524378
MSV3drs1057524378
GWAS Ctlgrs1057524378
Max Magnitude0
ClinVar
Risk rs1057524378(C;C)
Alt rs1057524378(C;C)
Reference Rs1057524378(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153579275A>G
CLNSRC
CLNACC RCV000430263.1,