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rs797045017

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045017(A;A)
Make rs797045017(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position83195936
GeneXRCC4
is asnp
is mentioned by
dbSNPrs797045017
ebirs797045017
HLIrs797045017
Exacrs797045017
Varsomers797045017
Maprs797045017
PheGenIrs797045017
hapmaprs797045017
1000 genomesrs797045017
hgdprs797045017
ensemblrs797045017
gopubmedrs797045017
geneviewrs797045017
scholarrs797045017
googlers797045017
pharmgkbrs797045017
gwascentralrs797045017
openSNPrs797045017
23andMers797045017
23andMe allrs797045017
SNP Nexus

SNPshotrs797045017
SNPdbers797045017
MSV3drs797045017
GWAS Ctlgrs797045017
Max Magnitude0
ClinVar
Risk rs797045017(A;A)
Alt rs797045017(A;A)
Reference rs797045017(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.82491755G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000190528.3,