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rs879255259

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255259(-;-)
Make rs879255259(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position83258544
GeneXRCC4
is asnp
is mentioned by
dbSNPrs879255259
ebirs879255259
HLIrs879255259
Exacrs879255259
Varsomers879255259
Maprs879255259
PheGenIrs879255259
hapmaprs879255259
1000 genomesrs879255259
hgdprs879255259
ensemblrs879255259
gopubmedrs879255259
geneviewrs879255259
scholarrs879255259
googlers879255259
pharmgkbrs879255259
gwascentralrs879255259
openSNPrs879255259
23andMers879255259
23andMe allrs879255259
SNP Nexus

SNPshotrs879255259
SNPdbers879255259
MSV3drs879255259
GWAS Ctlgrs879255259
Max Magnitude0
ClinVar
Risk rs879255259(;)
Alt rs879255259(;)
Reference rs879255259(G;G)
Significance Pathogenic
Disease Short stature
Variation info
Gene XRCC4
CLNDBN Short stature, microcephaly, and endocrine dysfunction
Reversed 0
HGVS NC_000005.9:g.82554363delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000190529.2,