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rs749466673

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749466673(A;A)
Make rs749466673(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132595041
GeneRAD50
is asnp
is mentioned by
dbSNPrs749466673
ebirs749466673
HLIrs749466673
Exacrs749466673
Varsomers749466673
Maprs749466673
PheGenIrs749466673
hapmaprs749466673
1000 genomesrs749466673
hgdprs749466673
ensemblrs749466673
gopubmedrs749466673
geneviewrs749466673
scholarrs749466673
googlers749466673
pharmgkbrs749466673
gwascentralrs749466673
openSNPrs749466673
23andMers749466673
23andMe allrs749466673
SNP Nexus

SNPshotrs749466673
SNPdbers749466673
MSV3drs749466673
GWAS Ctlgrs749466673
Max Magnitude0
ClinVar
Risk rs749466673(A;A)
Alt rs749466673(A;A)
Reference rs749466673(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene RAD50
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.131930733C>T
CLNSRC
CLNACC RCV000229634.1,