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rs1085307974

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position28845408
GeneMIR4721, SH2B1, TUFM
is asnp
is mentioned by
dbSNPrs1085307974
dbSNP (old)rs1085307974
ClinGenrs1085307974
ebirs1085307974
HLIrs1085307974
Exacrs1085307974
Gnomadrs1085307974
Varsomers1085307974
Maprs1085307974
PheGenIrs1085307974
Biobankrs1085307974
1000 genomesrs1085307974
hgdprs1085307974
ensemblrs1085307974
gopubmedrs1085307974
geneviewrs1085307974
scholarrs1085307974
googlers1085307974
pharmgkbrs1085307974
gwascentralrs1085307974
openSNPrs1085307974
23andMers1085307974
23andMe allrs1085307974
SNPshotrs1085307974
SNPdbers1085307974
MSV3drs1085307974
GWAS Ctlgrs1085307974
Max Magnitude0
ClinVar
Risk rs1085307974(C;C)
Alt rs1085307974(C;C)
Reference Rs1085307974(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SH2B1 TUFM NPIPB8 MIR4721
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.28856729C>G
CLNSRC
CLNACC RCV000489780.1,