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rs397507447

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507447(C;T)
Make rs397507447(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position101770182
GeneGNPTAB
is asnp
is mentioned by
dbSNPrs397507447
ebirs397507447
HLIrs397507447
Exacrs397507447
Varsomers397507447
Maprs397507447
PheGenIrs397507447
hapmaprs397507447
1000 genomesrs397507447
hgdprs397507447
ensemblrs397507447
gopubmedrs397507447
geneviewrs397507447
scholarrs397507447
googlers397507447
pharmgkbrs397507447
gwascentralrs397507447
openSNPrs397507447
23andMers397507447
23andMe allrs397507447
SNP Nexus

SNPshotrs397507447
SNPdbers397507447
MSV3drs397507447
GWAS Ctlgrs397507447
Max Magnitude0
ClinVar
Risk rs397507447(T;T)
Alt rs397507447(T;T)
Reference rs397507447(C;C)
Significance Pathogenic
Disease I cell disease not provided
Variation info
Gene GNPTAB
CLNDBN I cell disease not provided
Reversed 1
HGVS NC_000012.11:g.102163960G>A
CLNSRC HGMD
CLNACC RCV000032287.2, RCV000082186.3,