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rs149170427

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149170427(A;A)
Make rs149170427(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position37198797
GeneC5orf42
is asnp
is mentioned by
dbSNPrs149170427
dbSNP (old)rs149170427
ClinGenrs149170427
ebirs149170427
HLIrs149170427
Exacrs149170427
Gnomadrs149170427
Varsomers149170427
Maprs149170427
PheGenIrs149170427
Biobankrs149170427
1000 genomesrs149170427
hgdprs149170427
ensemblrs149170427
gopubmedrs149170427
geneviewrs149170427
scholarrs149170427
googlers149170427
pharmgkbrs149170427
gwascentralrs149170427
openSNPrs149170427
23andMers149170427
23andMe allrs149170427
SNPshotrs149170427
SNPdbers149170427
MSV3drs149170427
GWAS Ctlgrs149170427
Max Magnitude0
ClinVar
Risk rs149170427(A;A)
Alt rs149170427(A;A)
Reference Rs149170427(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C5orf42
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.37198899G>A
CLNSRC
CLNACC RCV000255984.1,