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rs1060501941

From SNPedia
Revision as of 19:03, 24 July 2017 by JlickBot (talk | contribs) (Update Rsnum - Set: Chromosome geno1 geno2 geno3 Gene position Gene_s Assembly GenomeBuild dbSNPBuild)
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Orientationplus
Stabilizedplus
Geno Mag Summary
(ACAC;ACAC) 0 common in clinvar
Make rs1060501941(-;-)
Make rs1060501941(-;CACA)
Make rs1060501941(CACA;CACA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132609389
GeneRAD50
is asnp
is mentioned by
dbSNPrs1060501941
dbSNP (classic)rs1060501941
ClinGenrs1060501941
ebirs1060501941
HLIrs1060501941
Exacrs1060501941
Gnomadrs1060501941
Varsomers1060501941
LitVarrs1060501941
Maprs1060501941
PheGenIrs1060501941
Biobankrs1060501941
1000 genomesrs1060501941
hgdprs1060501941
ensemblrs1060501941
geneviewrs1060501941
scholarrs1060501941
googlers1060501941
pharmgkbrs1060501941
gwascentralrs1060501941
openSNPrs1060501941
23andMers1060501941
SNPshotrs1060501941
SNPdbers1060501941
MSV3drs1060501941
GWAS Ctlgrs1060501941
Max Magnitude0
ClinVar
Risk rs1060501941(-;-)
Alt rs1060501941(-;-)
Reference Rs1060501941(ACAC;ACAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131945081_131945084delCACA
CLNSRC
CLNACC RCV000472041.1,


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