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rs1085307929

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome6
Position49453751
GeneMUT
is asnp
is mentioned by
dbSNPrs1085307929
dbSNP (old)rs1085307929
ClinGenrs1085307929
ebirs1085307929
HLIrs1085307929
Exacrs1085307929
Gnomadrs1085307929
Varsomers1085307929
Maprs1085307929
PheGenIrs1085307929
Biobankrs1085307929
1000 genomesrs1085307929
hgdprs1085307929
ensemblrs1085307929
gopubmedrs1085307929
geneviewrs1085307929
scholarrs1085307929
googlers1085307929
pharmgkbrs1085307929
gwascentralrs1085307929
openSNPrs1085307929
23andMers1085307929
23andMe allrs1085307929
SNPshotrs1085307929
SNPdbers1085307929
MSV3drs1085307929
GWAS Ctlgrs1085307929
Max Magnitude0
ClinVar
Risk rs1085307929(A;A)
Alt rs1085307929(A;A)
Reference Rs1085307929(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.49421464G>T
CLNSRC
CLNACC RCV000489403.1,