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rs7097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs7097(A;A)
Make rs7097(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27623299
GenePOLR1D
is asnp
is mentioned by
dbSNPrs7097
dbSNP (old)rs7097
ClinGenrs7097
ebirs7097
HLIrs7097
Exacrs7097
Gnomadrs7097
Varsomers7097
Maprs7097
PheGenIrs7097
Biobankrs7097
1000 genomesrs7097
hgdprs7097
ensemblrs7097
gopubmedrs7097
geneviewrs7097
scholarrs7097
googlers7097
pharmgkbrs7097
gwascentralrs7097
openSNPrs7097
23andMers7097
23andMe allrs7097
SNP Nexus

SNPshotrs7097
SNPdbers7097
MSV3drs7097
GWAS Ctlgrs7097
GMAF0.3503
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 21471979] Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility


ClinVar
Risk rs7097(A;A)
Alt rs7097(A;A)
Reference Rs7097(G;G)
Significance Non-pathogenic
Disease Treacher Collins Syndrome
Variation info
Gene POLR1D
CLNDBN Treacher Collins Syndrome, Dominant
Reversed 1
HGVS NC_000013.10:g.28197436C>T
CLNSRC
CLNACC RCV000273409.1,