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rs1064795342

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position49831396
GeneMED25, MIR6800
is asnp
is mentioned by
dbSNPrs1064795342
dbSNP (old)rs1064795342
ClinGenrs1064795342
ebirs1064795342
HLIrs1064795342
Exacrs1064795342
Gnomadrs1064795342
Varsomers1064795342
Maprs1064795342
PheGenIrs1064795342
Biobankrs1064795342
1000 genomesrs1064795342
hgdprs1064795342
ensemblrs1064795342
gopubmedrs1064795342
geneviewrs1064795342
scholarrs1064795342
googlers1064795342
pharmgkbrs1064795342
gwascentralrs1064795342
openSNPrs1064795342
23andMers1064795342
23andMe allrs1064795342
SNPshotrs1064795342
SNPdbers1064795342
MSV3drs1064795342
GWAS Ctlgrs1064795342
Max Magnitude0
ClinVar
Risk rs1064795342(-;-)
Alt rs1064795342(-;-)
Reference Rs1064795342(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MED25 MIR6800
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.50334653delC
CLNSRC
CLNACC RCV000479883.1,