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rs1057520515

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520515(A;A)
Make rs1057520515(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position2680321
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs1057520515
dbSNP (old)rs1057520515
ClinGenrs1057520515
ebirs1057520515
HLIrs1057520515
Exacrs1057520515
Gnomadrs1057520515
Varsomers1057520515
Maprs1057520515
PheGenIrs1057520515
Biobankrs1057520515
1000 genomesrs1057520515
hgdprs1057520515
ensemblrs1057520515
gopubmedrs1057520515
geneviewrs1057520515
scholarrs1057520515
googlers1057520515
pharmgkbrs1057520515
gwascentralrs1057520515
openSNPrs1057520515
23andMers1057520515
23andMe allrs1057520515
SNPshotrs1057520515
SNPdbers1057520515
MSV3drs1057520515
GWAS Ctlgrs1057520515
Max Magnitude0
ClinVar
Risk rs1057520515(A;A)
Alt rs1057520515(A;A)
Reference Rs1057520515(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PAFAH1B1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.2583615G>A
CLNSRC
CLNACC RCV000424252.1,