NM_000602.5:c.-820G[(4_5)]

HGVS Expressions

  • NG_013213.1:g.4332dup
  • NM_000602.5:c.-820G[(4_5)]
  • NC_000007.14:g.101126429dup
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Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Likely Benign, Risk factor

Variant Type

Indel

dbSNP

1799762

Clinvar

13572

Epidemiology in the Arab World

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