chrX:153760508:> Detail (hg19) (G6PD)

Information

Genome

Assembly Position
hg19 chrX:153,760,508-153,760,508
hg38 chrX:154,532,293-154,532,293 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Benign 2022-02-18 criteria provided, single submitter not provided germline Detail
Benign 2022-08-12 criteria provided, single submitter Anemia, nonspherocytic hemolytic, due to G6PD deficiency unknown Detail
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
NM_001360016.2(G6PD):c.1365-13C>T AND not provided ClinVar Detail
NM_001360016.2(G6PD):c.1365-13C>T AND Anemia, nonspherocytic hemolytic, due to G6PD deficiency ClinVar Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chrX:153,760,508-153,760,508
Variant Type
snv
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