Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519413

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519413(A;A)
Make rs1057519413(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position40729955
GeneRAD51
is asnp
is mentioned by
dbSNPrs1057519413
dbSNP (old)rs1057519413
ClinGenrs1057519413
ebirs1057519413
HLIrs1057519413
Exacrs1057519413
Gnomadrs1057519413
Varsomers1057519413
Maprs1057519413
PheGenIrs1057519413
Biobankrs1057519413
1000 genomesrs1057519413
hgdprs1057519413
ensemblrs1057519413
gopubmedrs1057519413
geneviewrs1057519413
scholarrs1057519413
googlers1057519413
pharmgkbrs1057519413
gwascentralrs1057519413
openSNPrs1057519413
23andMers1057519413
23andMe allrs1057519413
SNPshotrs1057519413
SNPdbers1057519413
MSV3drs1057519413
GWAS Ctlgrs1057519413
Max Magnitude0
ClinVar
Risk rs1057519413(A;A)
Alt rs1057519413(A;A)
Reference Rs1057519413(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene RAD51
CLNDBN Fanconi anemia, complementation group R
Reversed 0
HGVS NC_000015.9:g.41022153G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000412566.1,