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rs878855162

From SNPedia

Orientationminus
Geno Mag Summary
(GAGC;GAGC) 0 common in clinvar
Make rs878855162(-;-)
Make rs878855162(-;GAGC)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position3589909
GeneSLX4
is asnp
is mentioned by
dbSNPrs878855162
ebirs878855162
HLIrs878855162
Exacrs878855162
Varsomers878855162
Maprs878855162
PheGenIrs878855162
hapmaprs878855162
1000 genomesrs878855162
hgdprs878855162
ensemblrs878855162
gopubmedrs878855162
geneviewrs878855162
scholarrs878855162
googlers878855162
pharmgkbrs878855162
gwascentralrs878855162
openSNPrs878855162
23andMers878855162
23andMe allrs878855162
SNP Nexus

SNPshotrs878855162
SNPdbers878855162
MSV3drs878855162
GWAS Ctlgrs878855162
Max Magnitude0
ClinVar
Risk rs878855162(;)
Alt rs878855162(;)
Reference rs878855162(GAGC;GAGC)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene SLX4
CLNDBN Fanconi anemia
Reversed 1
HGVS NC_000016.9:g.3639910_3639913delGCTC
CLNSRC
CLNACC RCV000229151.1,