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rs869320677

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320677(-;-)
Make rs869320677(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position83104944
GeneXRCC4
is asnp
is mentioned by
dbSNPrs869320677
ebirs869320677
HLIrs869320677
Exacrs869320677
Varsomers869320677
Maprs869320677
PheGenIrs869320677
hapmaprs869320677
1000 genomesrs869320677
hgdprs869320677
ensemblrs869320677
gopubmedrs869320677
geneviewrs869320677
scholarrs869320677
googlers869320677
pharmgkbrs869320677
gwascentralrs869320677
openSNPrs869320677
23andMers869320677
23andMe allrs869320677
SNP Nexus

SNPshotrs869320677
SNPdbers869320677
MSV3drs869320677
GWAS Ctlgrs869320677
Max Magnitude0
ClinVar
Risk rs869320677(;)
Alt rs869320677(;)
Reference rs869320677(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.82400763delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000190522.2,