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rs397509404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509404(-;-)
Make rs397509404(-;A)
Make rs397509404(A;A)
ReferenceGRCh38 38.1/141
Chromosome16
Position13935662
GeneERCC4
is asnp
is mentioned by
dbSNPrs397509404
ebirs397509404
HLIrs397509404
Exacrs397509404
Varsomers397509404
Maprs397509404
PheGenIrs397509404
hapmaprs397509404
1000 genomesrs397509404
hgdprs397509404
ensemblrs397509404
gopubmedrs397509404
geneviewrs397509404
scholarrs397509404
googlers397509404
pharmgkbrs397509404
gwascentralrs397509404
openSNPrs397509404
23andMers397509404
23andMe allrs397509404
SNP Nexus

SNPshotrs397509404
SNPdbers397509404
MSV3drs397509404
GWAS Ctlgrs397509404
Max Magnitude0
ClinVar
Risk rs397509404(A;A)
Alt rs397509404(A;A)
Reference rs397509404(;)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene ERCC4
CLNDBN Xeroderma pigmentosum, type f/Cockayne syndrome
Reversed 0
HGVS NC_000016.9:g.14029519dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000049249.24,