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rs869320685

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320685(-;-)
Make rs869320685(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position58204171
GeneFANCL
is asnp
is mentioned by
dbSNPrs869320685
ebirs869320685
HLIrs869320685
Exacrs869320685
Varsomers869320685
Maprs869320685
PheGenIrs869320685
hapmaprs869320685
1000 genomesrs869320685
hgdprs869320685
ensemblrs869320685
gopubmedrs869320685
geneviewrs869320685
scholarrs869320685
googlers869320685
pharmgkbrs869320685
gwascentralrs869320685
openSNPrs869320685
23andMers869320685
23andMe allrs869320685
SNP Nexus

SNPshotrs869320685
SNPdbers869320685
MSV3drs869320685
GWAS Ctlgrs869320685
Max Magnitude0
ClinVar
Risk rs869320685(;)
Alt rs869320685(;)
Reference rs869320685(T;T)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene FANCL
CLNDBN Fanconi anemia, complementation group L
Reversed 1
HGVS NC_000002.11:g.58431306delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000191023.2,