Variant: 17:43072546 C / T

Warning! This variant is only covered in 462 individuals (adjusted allele number = 924).
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
chr17_43072546_C_T
Allele Frequency
0.001082
Allele Count
1 / 924
UCSC
17-43072546-C-T
ClinVar
Click to search for variant in Clinvar
Heterozygote Number
1
Homozygote Number
0
 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:

Note: This list may not include additional transcripts in the same gene that the variant does not overlap.
Population Frequencies
Population Frequency
Miao 0
Yao 0
Dong 0
Bouyei 0
Gelao 0
Zhuang 0
Sui 0
Yi 0.0125
Bai 0
Tujia 0
Hui 0
Total 0.00108225
Population Frequency
Africa/African-American N/A
Ashkenazi Jewish N/A
East Asian N/A
Finnish N/A
Non-Finnish European N/A
OTH N/A
Population Frequency
Africa/African-American N/A
Admixed American/Latino N/A
East Asian N/A
European N/A

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