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rs878855177

From SNPedia

Orientationplus
Geno Mag Summary
(TAACGA;TAACGA) 0 common in clinvar
Make rs878855177(CTAAG;CTAAG)
Make rs878855177(CTAAG;TAACGA)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position58692790
GeneRAD51C, TEX14
is asnp
is mentioned by
dbSNPrs878855177
ebirs878855177
HLIrs878855177
Exacrs878855177
Varsomers878855177
Maprs878855177
PheGenIrs878855177
hapmaprs878855177
1000 genomesrs878855177
hgdprs878855177
ensemblrs878855177
gopubmedrs878855177
geneviewrs878855177
scholarrs878855177
googlers878855177
pharmgkbrs878855177
gwascentralrs878855177
openSNPrs878855177
23andMers878855177
23andMe allrs878855177
SNP Nexus

SNPshotrs878855177
SNPdbers878855177
MSV3drs878855177
GWAS Ctlgrs878855177
Max Magnitude0
ClinVar
Risk rs878855177(CTAAG;CTAAG)
Alt rs878855177(CTAAG;CTAAG)
Reference rs878855177(TAACGA;TAACGA)
Significance Probable-Pathogenic
Disease Fanconi anemia
Variation info
Gene TEX14 RAD51C
CLNDBN Fanconi anemia, complementation group O
Reversed 0
HGVS NC_000017.10:g.56770151_56770156delTAACGAinsCTAAG
CLNSRC
CLNACC RCV000229481.1,