119775971
3:46898445
3:46898445
A
T/A/C
Not specified
Not specified
-
SNP
dbSNP
Frequency~Phenotype_or_Disease~ExAC~gnomAD
pathogenic
missense variant
V/E
204
204
1
deleterious
0
993
probably damaging
992
28001
likely benign
28
587
likely disease causing
586
364
tolerated
363
889
medium
888
ENST00000313049.9

Creators
Not specifiedSubmitter
Views: 131
Created: 16th Jun 2021 at 11:05

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