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rs1085307979

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position113149155
GeneF10, LOC102724474
is asnp
is mentioned by
dbSNPrs1085307979
dbSNP (old)rs1085307979
ClinGenrs1085307979
ebirs1085307979
HLIrs1085307979
Exacrs1085307979
Gnomadrs1085307979
Varsomers1085307979
Maprs1085307979
PheGenIrs1085307979
Biobankrs1085307979
1000 genomesrs1085307979
hgdprs1085307979
ensemblrs1085307979
gopubmedrs1085307979
geneviewrs1085307979
scholarrs1085307979
googlers1085307979
pharmgkbrs1085307979
gwascentralrs1085307979
openSNPrs1085307979
23andMers1085307979
23andMe allrs1085307979
SNPshotrs1085307979
SNPdbers1085307979
MSV3drs1085307979
GWAS Ctlgrs1085307979
Max Magnitude0
ClinVar
Risk rs1085307979(A;A)
Alt rs1085307979(A;A)
Reference Rs1085307979(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene F10
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.113803469G>A
CLNSRC
CLNACC RCV000489706.1,