RS9536062 THSD1
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What This Variant Does
"aka c.670C>
Associated Conditions
Non-immune hydrops fetalis
Lymphatic malformation 13
Non-immune hydrops fetalis
Lymphatic malformation 13
ClinVar Assertions (1)
NM_018676.4(THSD1):c.670C>T (p.Arg224Ter)
Population Frequencies
gnomAD ALL
0%
1kG AFR
89.6%
1kG ALL
94.7%
1kG AMR
97.4%
1kG EAS
99.2%
1kG EUR
96.1%
1kG SAS
93.5%
Other Variants in THSD1