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rs797045738

From SNPedia

Orientationplus
Make rs797045738(-;-)
Make rs797045738(-;AA)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position13078627
GeneNFIX
is asnp
is mentioned by
dbSNPrs797045738
ebirs797045738
HLIrs797045738
Exacrs797045738
Varsomers797045738
Maprs797045738
PheGenIrs797045738
hapmaprs797045738
1000 genomesrs797045738
hgdprs797045738
ensemblrs797045738
gopubmedrs797045738
geneviewrs797045738
scholarrs797045738
googlers797045738
pharmgkbrs797045738
gwascentralrs797045738
openSNPrs797045738
23andMers797045738
23andMe allrs797045738
SNP Nexus

SNPshotrs797045738
SNPdbers797045738
MSV3drs797045738
GWAS Ctlgrs797045738
Max Magnitude
ClinVar
Risk rs797045738(;)
Alt rs797045738(;)
Reference rs797045738(AA;AA)
Significance Pathogenic
Disease Marshall-Smith syndrome
Variation info
Gene NFIX
CLNDBN Marshall-Smith syndrome
Reversed 0
HGVS NC_000019.9:g.13189441_13189442delAA
CLNSRC
CLNACC RCV000194821.1,