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rs1057519148

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519148(A;G)
Make rs1057519148(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position115059864
GeneTNC
is asnp
is mentioned by
dbSNPrs1057519148
dbSNP (old)rs1057519148
ClinGenrs1057519148
ebirs1057519148
HLIrs1057519148
Exacrs1057519148
Gnomadrs1057519148
Varsomers1057519148
Maprs1057519148
PheGenIrs1057519148
Biobankrs1057519148
1000 genomesrs1057519148
hgdprs1057519148
ensemblrs1057519148
gopubmedrs1057519148
geneviewrs1057519148
scholarrs1057519148
googlers1057519148
pharmgkbrs1057519148
gwascentralrs1057519148
openSNPrs1057519148
23andMers1057519148
23andMe allrs1057519148
SNPshotrs1057519148
SNPdbers1057519148
MSV3drs1057519148
GWAS Ctlgrs1057519148
Max Magnitude0
ClinVar
Risk rs1057519148(G;G)
Alt rs1057519148(G;G)
Reference Rs1057519148(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNC
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.117822143T>C
CLNSRC
CLNACC RCV000415906.1,