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rs149587849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149587849(A;A)
Make rs149587849(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position225922042
GeneMIR6741, PYCR2
is asnp
is mentioned by
dbSNPrs149587849
dbSNP (old)rs149587849
ClinGenrs149587849
ebirs149587849
HLIrs149587849
Exacrs149587849
Gnomadrs149587849
Varsomers149587849
Maprs149587849
PheGenIrs149587849
Biobankrs149587849
1000 genomesrs149587849
hgdprs149587849
ensemblrs149587849
gopubmedrs149587849
geneviewrs149587849
scholarrs149587849
googlers149587849
pharmgkbrs149587849
gwascentralrs149587849
openSNPrs149587849
23andMers149587849
23andMe allrs149587849
SNPshotrs149587849
SNPdbers149587849
MSV3drs149587849
GWAS Ctlgrs149587849
Max Magnitude0
ClinVar
Risk rs149587849(A;A)
Alt rs149587849(A;A)
Reference Rs149587849(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PYCR2 MIR6741
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.226109742C>T
CLNSRC
CLNACC RCV000492990.1,