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rs756367276

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs756367276(-;-)
Make rs756367276(-;A)
Make rs756367276(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position89761961
GeneFANCA
is asnp
is mentioned by
dbSNPrs756367276
ebirs756367276
HLIrs756367276
Exacrs756367276
Varsomers756367276
Maprs756367276
PheGenIrs756367276
hapmaprs756367276
1000 genomesrs756367276
hgdprs756367276
ensemblrs756367276
gopubmedrs756367276
geneviewrs756367276
scholarrs756367276
googlers756367276
pharmgkbrs756367276
gwascentralrs756367276
openSNPrs756367276
23andMers756367276
23andMe allrs756367276
SNP Nexus

SNPshotrs756367276
SNPdbers756367276
MSV3drs756367276
GWAS Ctlgrs756367276
Max Magnitude0
ClinVar
Risk rs756367276(A;A)
Alt rs756367276(A;A)
Reference rs756367276(;)
Significance Pathogenic
Disease Fanconi anemia Fanconi anemia
Variation info
Gene FANCA
CLNDBN Fanconi anemia Fanconi anemia, complementation group A
Reversed 0
HGVS NC_000016.9:g.89828370dupA
CLNSRC
CLNACC RCV000168438.2, RCV000239378.1,