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rs869320678

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320678(G;T)
Make rs869320678(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position83104909
GeneXRCC4
is asnp
is mentioned by
dbSNPrs869320678
ebirs869320678
HLIrs869320678
Exacrs869320678
Varsomers869320678
Maprs869320678
PheGenIrs869320678
hapmaprs869320678
1000 genomesrs869320678
hgdprs869320678
ensemblrs869320678
gopubmedrs869320678
geneviewrs869320678
scholarrs869320678
googlers869320678
pharmgkbrs869320678
gwascentralrs869320678
openSNPrs869320678
23andMers869320678
23andMe allrs869320678
SNP Nexus

SNPshotrs869320678
SNPdbers869320678
MSV3drs869320678
GWAS Ctlgrs869320678
Max Magnitude0
ClinVar
Risk rs869320678(T;T)
Alt rs869320678(T;T)
Reference rs869320678(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.82400728G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190524.2,