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rs724159986

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs724159986(-;-)
Make rs724159986(-;A)
Make rs724159986(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position40729933
GeneRAD51
is asnp
is mentioned by
dbSNPrs724159986
ebirs724159986
HLIrs724159986
Exacrs724159986
Varsomers724159986
Maprs724159986
PheGenIrs724159986
hapmaprs724159986
1000 genomesrs724159986
hgdprs724159986
ensemblrs724159986
gopubmedrs724159986
geneviewrs724159986
scholarrs724159986
googlers724159986
pharmgkbrs724159986
gwascentralrs724159986
openSNPrs724159986
23andMers724159986
23andMe allrs724159986
SNP Nexus

SNPshotrs724159986
SNPdbers724159986
MSV3drs724159986
GWAS Ctlgrs724159986
Max Magnitude0
ClinVar
Risk rs724159986(A;A)
Alt rs724159986(A;A)
Reference rs724159986(;)
Significance Pathogenic
Disease Mirror movements 2
Variation info
Gene RAD51
CLNDBN Mirror movements 2
Reversed 0
HGVS NC_000015.9:g.41022131dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000022748.26,