GENETIC ENCYCLOPEDIA
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NM_000101.4(CYBA):c.203+8T>C AND not specified

Significance: Benign
ClinVar: RCV000176978

Variant: NM_000101.4(CYBA):c.203+8T>C

Type: Variant
Allele: NM_000101.4(CYBA):c.203+8T>C 193368
Gene:
Type: single nucleotide variant
Location: Chr16: 88713501 - assembly GRCh37
Chr16: 88647093 - assembly GRCh38
References: dbSNP: 4782393

Condition

Disease: not specified