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rs779773463

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779773463(C;T)
Make rs779773463(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position83195935
GeneXRCC4
is asnp
is mentioned by
dbSNPrs779773463
ebirs779773463
HLIrs779773463
Exacrs779773463
Varsomers779773463
Maprs779773463
PheGenIrs779773463
hapmaprs779773463
1000 genomesrs779773463
hgdprs779773463
ensemblrs779773463
gopubmedrs779773463
geneviewrs779773463
scholarrs779773463
googlers779773463
pharmgkbrs779773463
gwascentralrs779773463
openSNPrs779773463
23andMers779773463
23andMe allrs779773463
SNP Nexus

SNPshotrs779773463
SNPdbers779773463
MSV3drs779773463
GWAS Ctlgrs779773463
Max Magnitude0
ClinVar
Risk rs779773463(T;T)
Alt rs779773463(T;T)
Reference rs779773463(C;C)
Significance Pathogenic
Disease Short stature
Variation info
Gene XRCC4
CLNDBN Short stature, microcephaly, and endocrine dysfunction
Reversed 0
HGVS NC_000005.9:g.82491754C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190526.2,