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rs397509400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AACTC;AACTC) 0 common in clinvar
(CTCAA;CTCAA) 0 common in clinvar
Make rs397509400(-;-)
Make rs397509400(-;CTCAA)
ReferenceGRCh38 38.1/141
Chromosome16
Position13935416
GeneERCC4
is asnp
is mentioned by
dbSNPrs397509400
ebirs397509400
HLIrs397509400
Exacrs397509400
Varsomers397509400
Maprs397509400
PheGenIrs397509400
hapmaprs397509400
1000 genomesrs397509400
hgdprs397509400
ensemblrs397509400
gopubmedrs397509400
geneviewrs397509400
scholarrs397509400
googlers397509400
pharmgkbrs397509400
gwascentralrs397509400
openSNPrs397509400
23andMers397509400
23andMe allrs397509400
SNP Nexus

SNPshotrs397509400
SNPdbers397509400
MSV3drs397509400
GWAS Ctlgrs397509400
Max Magnitude0
ClinVar
Risk rs397509400(;)
Alt rs397509400(;)
Reference rs397509400(AACTC;AACTC)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene ERCC4
CLNDBN Fanconi anemia, complementation group Q
Reversed 0
HGVS NC_000016.9:g.14029273_14029277delCTCAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000049244.25,