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rs587777612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777612(C;C)
Make rs587777612(C;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position124346784
GeneSH2D1A
is asnp
is mentioned by
dbSNPrs587777612
ebirs587777612
HLIrs587777612
Exacrs587777612
Varsomers587777612
Maprs587777612
PheGenIrs587777612
hapmaprs587777612
1000 genomesrs587777612
hgdprs587777612
ensemblrs587777612
gopubmedrs587777612
geneviewrs587777612
scholarrs587777612
googlers587777612
pharmgkbrs587777612
gwascentralrs587777612
openSNPrs587777612
23andMers587777612
23andMe allrs587777612
SNP Nexus

SNPshotrs587777612
SNPdbers587777612
MSV3drs587777612
GWAS Ctlgrs587777612
Max Magnitude0
ClinVar
Risk rs587777612(C;C)
Alt rs587777612(C;C)
Reference rs587777612(G;G)
Significance Pathogenic
Disease Lymphoproliferative syndrome 1
Variation info
Gene SH2D1A
CLNDBN Lymphoproliferative syndrome 1, X-linked
Reversed 0
HGVS NC_000023.10:g.123480634G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133459.3,