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

rs1057518160

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518160(A;A)
Make rs1057518160(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position154988140
GeneFLAD1
is asnp
is mentioned by
dbSNPrs1057518160
dbSNP (old)rs1057518160
ClinGenrs1057518160
ebirs1057518160
HLIrs1057518160
Exacrs1057518160
Gnomadrs1057518160
Varsomers1057518160
Maprs1057518160
PheGenIrs1057518160
Biobankrs1057518160
1000 genomesrs1057518160
hgdprs1057518160
ensemblrs1057518160
gopubmedrs1057518160
geneviewrs1057518160
scholarrs1057518160
googlers1057518160
pharmgkbrs1057518160
gwascentralrs1057518160
openSNPrs1057518160
23andMers1057518160
23andMe allrs1057518160
SNPshotrs1057518160
SNPdbers1057518160
MSV3drs1057518160
GWAS Ctlgrs1057518160
Max Magnitude0
ClinVar
Risk rs1057518160(A;A)
Alt rs1057518160(A;A)
Reference Rs1057518160(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLAD1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.154960616C>A
CLNSRC
CLNACC RCV000414135.1,