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Variant:
9:97793827 G / A
dbSNP
rs965513
UCSC
chr9:97793827:A:G
gnomAD
chr9:97793827:A:G
ClinVar
Click to search for variant in Clinvar
Annotations
This variant falls on 8 transcripts in 1 genes:
intron
PTCSC2
Transcripts
ENST00000430058
ENST00000648027
ENST00000648505
ENST00000648625
ENST00000649253
ENST00000649461
ENST00000649526
ENST00000650104
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