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rs879255258

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255258(G;G)
Make rs879255258(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position83111134
GeneXRCC4
is asnp
is mentioned by
dbSNPrs879255258
ebirs879255258
HLIrs879255258
Exacrs879255258
Varsomers879255258
Maprs879255258
PheGenIrs879255258
hapmaprs879255258
1000 genomesrs879255258
hgdprs879255258
ensemblrs879255258
gopubmedrs879255258
geneviewrs879255258
scholarrs879255258
googlers879255258
pharmgkbrs879255258
gwascentralrs879255258
openSNPrs879255258
23andMers879255258
23andMe allrs879255258
SNP Nexus

SNPshotrs879255258
SNPdbers879255258
MSV3drs879255258
GWAS Ctlgrs879255258
Max Magnitude0
ClinVar
Risk rs879255258(G;G)
Alt rs879255258(G;G)
Reference rs879255258(T;T)
Significance Pathogenic
Disease Short stature
Variation info
Gene XRCC4
CLNDBN Short stature, microcephaly, and endocrine dysfunction
Reversed 0
HGVS NC_000005.9:g.82406953T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000190527.3,