ClinVar Miner

List of variants studied for Prader-Willi syndrome by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_004667.5(HERC2):c.13612G>A (p.Val4538Met) rs149338352
NM_019066.5(MAGEL2):c.1715C>T (p.Ala572Val) rs1064797195
NM_019066.5(MAGEL2):c.1912C>T (p.Gln638Ter) rs797044883
NM_019066.5(MAGEL2):c.3017C>G (p.Thr1006Ser) rs138628273

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