Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517775

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517775(A;A)
Make rs1057517775(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position183586894
GeneNCF2
is asnp
is mentioned by
dbSNPrs1057517775
dbSNP (old)rs1057517775
ClinGenrs1057517775
ebirs1057517775
HLIrs1057517775
Exacrs1057517775
Gnomadrs1057517775
Varsomers1057517775
Maprs1057517775
PheGenIrs1057517775
Biobankrs1057517775
1000 genomesrs1057517775
hgdprs1057517775
ensemblrs1057517775
gopubmedrs1057517775
geneviewrs1057517775
scholarrs1057517775
googlers1057517775
pharmgkbrs1057517775
gwascentralrs1057517775
openSNPrs1057517775
23andMers1057517775
23andMe allrs1057517775
SNPshotrs1057517775
SNPdbers1057517775
MSV3drs1057517775
GWAS Ctlgrs1057517775
Max Magnitude0
ClinVar
Risk rs1057517775(A;A)
Alt rs1057517775(A;A)
Reference Rs1057517775(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NCF2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.183556029C>T
CLNSRC
CLNACC RCV000412920.1,