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rs786205522

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205522(A;T)
Make rs786205522(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position39058794
GeneSOS1
is asnp
is mentioned by
dbSNPrs786205522
ebirs786205522
HLIrs786205522
Exacrs786205522
Varsomers786205522
Maprs786205522
PheGenIrs786205522
hapmaprs786205522
1000 genomesrs786205522
hgdprs786205522
ensemblrs786205522
gopubmedrs786205522
geneviewrs786205522
scholarrs786205522
googlers786205522
pharmgkbrs786205522
gwascentralrs786205522
openSNPrs786205522
23andMers786205522
23andMe allrs786205522
SNP Nexus

SNPshotrs786205522
SNPdbers786205522
MSV3drs786205522
GWAS Ctlgrs786205522
Max Magnitude0
ClinVar
Risk rs786205522(T;T)
Alt rs786205522(T;T)
Reference rs786205522(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.39285935T>A
CLNSRC
CLNACC RCV000171289.1,