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rs786205515

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205515(G;T)
Make rs786205515(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position13025513
GeneNFIX
is asnp
is mentioned by
dbSNPrs786205515
ebirs786205515
HLIrs786205515
Exacrs786205515
Varsomers786205515
Maprs786205515
PheGenIrs786205515
hapmaprs786205515
1000 genomesrs786205515
hgdprs786205515
ensemblrs786205515
gopubmedrs786205515
geneviewrs786205515
scholarrs786205515
googlers786205515
pharmgkbrs786205515
gwascentralrs786205515
openSNPrs786205515
23andMers786205515
23andMe allrs786205515
SNP Nexus

SNPshotrs786205515
SNPdbers786205515
MSV3drs786205515
GWAS Ctlgrs786205515
Max Magnitude0
ClinVar
Risk rs786205515(T;T)
Alt rs786205515(T;T)
Reference rs786205515(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NFIX
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13136327G>T
CLNSRC
CLNACC RCV000171277.1,