ClinVar Miner

Submissions for variant NM_002025.4(AFF2):c.3448G>T (p.Asp1150Tyr)

gnomAD frequency: 0.00001  dbSNP: rs781818996
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biological Sciences, International Islamic University, Islamabad RCV001251517 SCV001423533 pathogenic FRAXE 2018-10-16 no assertion criteria provided clinical testing

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