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rs574088829

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs574088829(A;A)
Make rs574088829(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position39012319
GeneSOS1
is asnp
is mentioned by
dbSNPrs574088829
ebirs574088829
HLIrs574088829
Exacrs574088829
Varsomers574088829
Maprs574088829
PheGenIrs574088829
hapmaprs574088829
1000 genomesrs574088829
hgdprs574088829
ensemblrs574088829
gopubmedrs574088829
geneviewrs574088829
scholarrs574088829
googlers574088829
pharmgkbrs574088829
gwascentralrs574088829
openSNPrs574088829
23andMers574088829
23andMe allrs574088829
SNP Nexus

SNPshotrs574088829
SNPdbers574088829
MSV3drs574088829
GWAS Ctlgrs574088829
Max Magnitude0
ClinVar
Risk rs574088829(A,G;A,G)
Alt rs574088829(A,G;A,G)
Reference rs574088829(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SOS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.39239460T>A
CLNSRC
CLNACC RCV000159127.1,