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rs756998312

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756998312(A;A)
Make rs756998312(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152310100
GeneFLG
is asnp
is mentioned by
dbSNPrs756998312
dbSNP (classic)rs756998312
ClinGenrs756998312
ebirs756998312
HLIrs756998312
Exacrs756998312
Gnomadrs756998312
Varsomers756998312
LitVarrs756998312
Maprs756998312
PheGenIrs756998312
Biobankrs756998312
1000 genomesrs756998312
hgdprs756998312
ensemblrs756998312
geneviewrs756998312
scholarrs756998312
googlers756998312
pharmgkbrs756998312
gwascentralrs756998312
openSNPrs756998312
23andMers756998312
SNPshotrs756998312
SNPdbers756998312
MSV3drs756998312
GWAS Ctlgrs756998312
Max Magnitude0
ClinVar
Risk rs756998312(A;A) rs756998312(T;T)
Alt rs756998312(A;A) rs756998312(T;T)
Reference Rs756998312(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152282576G>A
CLNSRC
CLNACC RCV000323173.1,