95524920
3:46898691
3:46898691
G
A/G
Not specified
Not specified
-
SNP
dbSNP
Frequency~Cited~Phenotype_or_Disease
pathogenic
missense variant
H/R
223
223
1
deleterious
0
977
probably damaging
976
27001
likely benign
27
685
likely disease causing
684
514
damaging
513
983
high
982
ENST00000313049.9

Creators
Not specifiedSubmitter
Views: 152
Created: 16th Jun 2021 at 11:05

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