Variant: 17:43102588 C / T

Warning! This variant is only covered in 466 individuals (adjusted allele number = 932).
This means that the site is covered in fewer than 80% of the individuals in GMGD, which may indicate a low-quality site.

Genome build: GRCh37
Filter Status: PASS
dbSNP: rs708381
Allele Frequency: 0.2897
Allele Count: 270 / 932
UCSC: 17-43102588-C-T
ClinVar: Click to search for variant in Clinvar
Heterozygote Number: 136
Homozygote Number: 67

Site Quality Metrics

Note: These are site-level quality metrics: they may be unpredictable for multi-allelic sites.

Annotations

This variant falls on 1 transcripts in 1 genes:

intron

BRCA1 - ENST00000471181 *

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.

Population Frequencies

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Email: GMGD@service.genomics.cn

Variant: 17:43102588 C / T

Variant: 17:43102588 C / T

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