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rs200900510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200900510(C;T)
Make rs200900510(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position6329900
GeneTNFRSF1A
is asnp
is mentioned by
dbSNPrs200900510
dbSNP (classic)rs200900510
ClinGenrs200900510
ebirs200900510
HLIrs200900510
Exacrs200900510
Gnomadrs200900510
Varsomers200900510
LitVarrs200900510
Maprs200900510
PheGenIrs200900510
Biobankrs200900510
1000 genomesrs200900510
hgdprs200900510
ensemblrs200900510
geneviewrs200900510
scholarrs200900510
googlers200900510
pharmgkbrs200900510
gwascentralrs200900510
openSNPrs200900510
23andMers200900510
23andMe allrs200900510
SNPshotrs200900510
SNPdbers200900510
MSV3drs200900510
GWAS Ctlgrs200900510
Max Magnitude0
ClinVar
Risk rs200900510(T;T)
Alt rs200900510(T;T)
Reference Rs200900510(C;C)
Significance Pathogenic
Disease not specified Behcet's syndrome
Variation info
Gene TNFRSF1A
CLNDBN not specified Behcet's syndrome
Reversed 0
HGVS NC_000012.11:g.6439066C>T
CLNSRC
CLNACC RCV000419009.1, RCV000458191.1,