Rs104894535

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Orientationminus
is asnp
is mentioned by
dbSNPrs104894535
PheGenIrs104894535
nextbiors104894535
hapmaprs104894535
1000 genomesrs104894535
hgdprs104894535
ensemblrs104894535
gopubmedrs104894535
geneviewrs104894535
scholarrs104894535
googlers104894535
pharmgkbrs104894535
gwascentralrs104894535
openSNPrs104894535
23andMers104894535
23andMe allrs104894535
SNP Nexus

SNPshotrs104894535
SNPdbers104894535
MSV3drs104894535
GeneSALL1
Chromosome16
Orientationminus
Position51175018
ReferenceGRCh37 37.1/132
Max Magnitude0
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894535(C;G)
Make rs104894535(G;G)
OMIM602218
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894535(A,G;A,G)
Alt rs104894535(A,G;A,G)
Reference rs104894535(C;C)
Significance 5
Disease Townes syndrome
ClinVar info
Gene SALL1
CLNDBN Townes syndrome
Reversed 1
CLNHGVS NC_000016.9:g.51175018G>C; NC_000016.9:g.51175018G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007854.1, RCV000007852.1