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rs1057518626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518626(-;-)
Make rs1057518626(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154361786
GeneFLNA
is asnp
is mentioned by
dbSNPrs1057518626
dbSNP (old)rs1057518626
ClinGenrs1057518626
ebirs1057518626
HLIrs1057518626
Exacrs1057518626
Gnomadrs1057518626
Varsomers1057518626
Maprs1057518626
PheGenIrs1057518626
Biobankrs1057518626
1000 genomesrs1057518626
hgdprs1057518626
ensemblrs1057518626
gopubmedrs1057518626
geneviewrs1057518626
scholarrs1057518626
googlers1057518626
pharmgkbrs1057518626
gwascentralrs1057518626
openSNPrs1057518626
23andMers1057518626
23andMe allrs1057518626
SNPshotrs1057518626
SNPdbers1057518626
MSV3drs1057518626
GWAS Ctlgrs1057518626
Max Magnitude0
ClinVar
Risk rs1057518626(-;-)
Alt rs1057518626(-;-)
Reference Rs1057518626(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153590154delC
CLNSRC
CLNACC RCV000414405.1,