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rs1085307449

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TATC;TATC) 0 common in clinvar
Chromosome14
Position56633145
GeneLOC105370515, TMEM260
is asnp
is mentioned by
dbSNPrs1085307449
dbSNP (old)rs1085307449
ClinGenrs1085307449
ebirs1085307449
HLIrs1085307449
Exacrs1085307449
Gnomadrs1085307449
Varsomers1085307449
Maprs1085307449
PheGenIrs1085307449
Biobankrs1085307449
1000 genomesrs1085307449
hgdprs1085307449
ensemblrs1085307449
gopubmedrs1085307449
geneviewrs1085307449
scholarrs1085307449
googlers1085307449
pharmgkbrs1085307449
gwascentralrs1085307449
openSNPrs1085307449
23andMers1085307449
23andMe allrs1085307449
SNPshotrs1085307449
SNPdbers1085307449
MSV3drs1085307449
GWAS Ctlgrs1085307449
Max Magnitude0
ClinVar
Risk rs1085307449(-;-)
Alt rs1085307449(-;-)
Reference Rs1085307449(TATC;TATC)
Significance Pathogenic
Disease Structural heart defects and renal anomalies syndrome
Variation info
Gene TMEM260
CLNDBN Structural heart defects and renal anomalies syndrome
Reversed 0
HGVS NC_000014.8:g.57099863_57099866delCTAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000488879.1,